Methods for barcoding macromolecules in individual cells

ABSTRACT

The present disclosure relates to methods and kits for generating single cell barcodes and imparting them to the constituent molecules within a single cell. Additionally, methods to overlay sample barcode and spatial barcode information onto the single cell barcodes are also described. Generation of single cell barcodes is achieved by labeling the genomic DNA of a cell/nucleus with a small handful, preferably just a one or two cellular barcode probes (CBP) that can be amplified and propagated to label the constituent molecules within the cell. The disclosure finds utility in applications such as characterization of cellular heterogeneity, comprehensive profiling of tissue composition, characterization of adherent cells, discovery of new cell subtypes and functions of individual cells in the context of its microenvironment, and others.

CROSS-REFERENCE TO RELATED APPLICATION

This application claims priority to U.S. Provisional Patent ApplicationNo. 63/278,045 filed Nov. 10, 2021, entitled “METHODS FOR BARCODINGMACROMOLECULES IN INDIVIDUAL CELLS,” which is herein incorporated byreference in its entirety for all purposes.

REFERENCE TO AN ELECTRONIC SEQUENCE LISTING

The contents of the electronic sequence listing(776532003800SEQLIST.xml; Size: 16,666 bytes; and Date of Creation: Nov.9, 2022) is herein incorporated by reference in its entirety.

TECHNICAL FIELD

The present disclosure relates to biotechnology, and in some aspects tomethods and kits for barcoding macromolecules in individual cells usingcell barcode probes (CBPs) that comprise a common genome binding elementand a cell barcode. In some embodiments, the disclosure finds utility inapplications such as characterization of cellular heterogeneity,comprehensive profiling of tissue composition, characterization ofadherent cells, discovery of new cell subtypes and/or functions ofindividual cells in the context of its microenvironment, and others.

BACKGROUND

It has been increasingly accepted that seemingly homogeneous tissues orcell populations exhibit heterogeneity in gene expression and proteinlevels. In some situations, such as during cancer cell evolution, theDNA mutation and methylation profiles also differ among individualcells. Therefore, the ability to analyze DNA, RNA and protein at singlecell resolution is of great importance. Traditionally single cell mRNAand protein expression have been examined by fluorescent in situhybridization with a microscope (Kalisky, T. and Quake, S. R. (2011)Single cell genomics. Nat Methods, 8, 311-314) and flow cytometer (Wu,M. and Singh, A. K. (2012) Single cell protein analysis. Curr OpinBiotechnol, 23, 83-88), respectively. More recently, qPCR was employedfor single cell mRNA analysis (Dalerba, P., et al. (2011) Single celldissection of transcriptional heterogeneity in human colon tumors. NatBiotechnol, 29, 1120-1127). However, to obtain a more comprehensiveunderstanding of the complex molecular networks in the living cell, ahighly multiplexed approach is necessary. There remains a need forimproved techniques relating to multiplexing DNA, RNA and proteinmolecules as well as kits for accomplishing the same. The presentdisclosure addresses these and other needs.

SUMMARY

The summary is not intended to be used to limit the scope of the claimedsubject matter. Other features, details, utilities, and advantages ofthe claimed subject matter will be apparent from the detaileddescription including those aspects disclosed in the accompanyingdrawings and in the appended claims.

Next-generation sequencing (NGS) can be used for single cell analysis.The first single cell mRNA sequencing (mRNA-seq) study was published in2009 (Tang, F., et al. (2009) mRNA-Seq whole-transcriptome analysis of asingle cell. Nat Methods, 6, 377-382). Since then, this field has beenrevolutionized and various commercial single cell platforms have beendeveloped including: Fluidigm C1 (Pollen, A. A., et al. (2014)Low-coverage single cell mRNA sequencing reveals cellular heterogeneityand activated signaling pathways in developing cerebral cortex. NatBiotechnol, 32, 1053-1058, and Gong, H., et al. (2017) Single cellprotein-mRNA correlation analysis enabled by multiplexed dual-analyteco-detection. Sci Rep, 7, 2776); 10×Chromium (Zheng, G. X., et al.(2017); Massively parallel digital transcriptional profiling of singlecells. Nat Commun, 8, 14049); Mission Bio Tapestri (Demaree, B., et al.(2021); Joint profiling of DNA and proteins in single cells to dissectgenotype-phenotype associations in leukemia. Nat Commun, 12, 1583); andBD Rhapsody (Mair, F., (2020) et al. A Targeted Multi-omic AnalysisApproach Measures Protein Expression and Low-Abundance Transcripts onthe Single cell Level. Cell Rep, 31, 107499). Moreover, high throughputsingle cell analysis protocols that do not rely on a dedicated singlecell platforms but employ bulk processes to combinatorically barcodecell populations with single cell resolution have been developedincluding: SPLiT-seq (Rosenberg, A. B., et al. (2018) Single cellprofiling of the developing mouse brain and spinal cord with split-poolbarcoding. Science, 360, 176-182); and sci-RNA-seq (Cao, J., et al.(2017) Comprehensive single cell transcriptional profiling of amulticellular organism. Science, 357, 661-667).

Analyzing tissues and cells at single cell level can be used for avariety of applications such as characterization of cellularheterogeneity, profiling of tissue composition, discovery of new cellsubtypes, characterization of adherent cell types such as from a fluidbiopsy with relevant circulating tumor cells (CTCs) (Marrinucci, et al.,2012. “Fluid Biopsy in Patients with Metastatic Prostate, Pancreatic andBreast Cancers.” Physical Biology 9 (1): 016003), identification ofnovel marker genes, investigation of allelic expression patterns,dissection of gene-regulatory networks, study of T cell fate andclonality, and even production of cellular maps of entire cell lineages,organs and organisms (Mereu, E., et al. (2020) Benchmarking single cellRNA-sequencing protocols for cell atlas projects. Nat Biotechnol, 38,747-755). Thiele et al. describe the use of adherent high-density singlecell analysis (HD-SCA) using both cell-staining based morphologicalanalysis combined with single-cell genomic analysis to characterizedsubpopulations with relevance to cancer outcomes (Thiele, et al., 2019.“Single-Cell Analysis of Circulating Tumor Cells.” Methods in MolecularBiology 1908: 243-64). Adherent cell sample slides can also be createdby using a “touch prep” in which a resected tumor tissue or biopsyspecimen is lightly touched to the surface of a slide leaving a layer oftumor and associated cells on the surface of the slide in the context ofpreserving spatial information (Thiele et al., 2019).

The multi-omic analysis of CTCs in a collection of adherent cells suchas derived from a fluid biopsy is instrumental in providing diagnosticand prognostic information on tumor development and progression. In someembodiments, adherent cells can provide both phenotypic informationderived from cell (e.g., staining with dyes and fluorescent antibodies),and molecular information derived from multi-omic analysis, e.g., asdescribed in the present disclosure. In some embodiments, methods andcompositions disclosed herein can be used for characterizing CTCheterogeneity in a fluid biopsy and understanding its impact on cancerprogression.

Comprehensive analyses of heterogeneous cell populations requiredevelopment of simple and efficient methods for barcoding macromoleculesin individual cells. In some embodiments, provided herein are methods,compositions, and kits for multiplexing analytes, such as DNA, RNA andprotein molecules. In some embodiments, analytes are barcoded atcellular level. In some embodiments, the single cell barcoding methodsdisclosed herein can allow multiple analytes (e.g., DNA, RNA andprotein) from each single cell to be barcoded in a single assay with acell-specific barcode. The barcoding methods disclosed herein may beutilized in a wide variety of nucleic acid-based and/or protein-basedprocedures. In some embodiments, the present disclosure providesmolecular analysis using single cell barcoding described herein forsingle cell multi-omic analysis including genomic, transcriptomic, andproteomic analysis a cell sample or a tissue sample, including but notlimited to adherent cell samples for HD-SCA.

In some embodiments, disclosed herein is a method for barcodingmacromolecules of, in, and/or form a biological sample. In someembodiments, the biological sample comprises a plurality of cells and/ornuclei. The cells and/or nuclei of the biological sample may bedissociated cells and/or nuclei, for example, generated by dissociatinga tissue sample into dissociated single cells. In some embodiments, thebiological sample can be a tissue sample such as a tissue section ortissue block.

In some embodiments, a method disclosed herein can comprise contactingthe cells or nuclei in a biological sample with cell barcode probes orgenomic DNA-binding carriers carrying cell barcodes. In someembodiments, the specific genomic DNA-binding carrier comprises acatalytically inactive Cas nuclease, a TALE protein, or a zinc-fingerprotein.

In some embodiments, a given cell barcode probe comprises: i) a genomebinding element shared among the cell barcode probes, and ii) a cellbarcode. In some embodiments, the cell barcode is unique to the givencell barcode probe and identifies the given cell barcode probe fromamong the cell barcode probes.

In some embodiments, the genome binding element or genomic DNA-bindingcarrier shared among the cell barcode probes binds to a region in thegenomic DNA of the cells or nuclei. In some embodiments, the genomebinding element shared among the cell barcode probes comprises asequence that is complementary to a region in the genomic DNA (gDNA) ofthe cells or nuclei (e.g., the genome binding element can becomplementary to a DNA strand in a non-repetitive region in the gDNA.The non-repetitive region can be a unique region compared to otherregions in the gDNA, and the non-repetitive region can be shared by allor substantially all of the cells or nuclei of, in, and/or from thebiological sample. In some embodiments, the genome binding elementtargets a specific region in the gDNA of the cells or nuclei, where eachcell or nuclei comprises one or two copies of the specific region (suchas in a diploid cell. In some embodiments, the given cell barcode probefurther comprises a UMI that can be used to distinguish the particularcell barcode probe molecule from other cell barcode probe moleculeshaving the same cell barcode.

In some embodiments, the cells or nuclei can be contacted with the cellbarcode probes prior to, during, and/or after dissociating thebiological sample into dissociated single cells and/or nuclei. In someembodiments, the method can comprise permeabilizing the cells and/ornuclei, for instance, to facilitate binding of the cell barcode probesto the genomic DNA. In some embodiments, the method can comprise makinggenomic DNA of the cells and/or nuclei at least partially accessible tonucleic acid hybridization, for instance, to facilitate hybridization ofthe genome binding element or a portion thereof to a DNA strand of anon-repetitive region in the genomic DNA. In some embodiments, themethod comprises forming a nucleic acid duplex between the genomebinding element and the region of the genomic DNA in the cells and/ornuclei. In some embodiments, each cell or nucleus contains no more thana defined number of copies of the non-repetitive region, such as one ortwo copies, thereby limiting the number of cell barcode probe moleculesthat can bind to the genomic DNA of each cell or nucleus.

In some embodiments, the method comprises removing molecules of cellbarcode probes that are not bound or nonspecifically bound to thegenomic DNA from the cells and/or nuclei, whereby no more than a definednumber of cell barcode probe molecules (such as one or two molecules)remain in each cell or nucleus.

In some embodiments, the method comprises partitioning the cells and/ornuclei into a plurality of partitions (e.g., compartments, such asemulsion droplets or microwells). In some embodiments, each partitioncontains no more than one cell or nucleus. In some embodiments, eachpartition contains no more than a single cell or nucleus containing nomore than two cell barcode probe molecules specifically bound to thegenomic DNA of the single cell or nucleus. The no more than two cellbarcode probe molecules can comprise the shared genome binding elementand the cell barcode(s) unique to the cell barcode probe(s), andoptionally a UMI that is unique to each cell barcode probe molecule.

In some embodiments, the method comprises amplifying the cell barcode(s)within each partition of the plurality of partitions, thereby formingamplified oligonucleotides comprising cell barcodes within thepartition. Since in some embodiments for each cell or nucleus, the cellbarcode(s) in the cell or nucleus are unique among the plurality of cellbarcode probes (therefore distinguishing the cell or nucleus from othercells or nuclei that have received other unique cell barcodes), the cellbarcode(s) can be used to uniquely identify the cell or nucleus (andcomponents such as macromolecules thereof) from among the cells ornuclei of the biological sample.

In some embodiments, the method comprises attaching the amplified cellbarcodes in each partition to the macromolecules within the partition,thereby forming barcoded macromolecules. In some embodiments, since thebarcoded macromolecules comprise cell barcode(s) that can be used touniquely identify the cell or nucleus containing the macromolecules, thebarcoded macromolecules from different partitions (e.g., differentsingle cells or nuclei) can be pooled and analyzed in a high throughputmanner, comprising analyzing the cell barcodes (and optionally samplebarcodes, UMIs, and/or spatial barcodes) using NGS, thereby analyzingmacromolecules such as proteins of the biological sample on asingle-cell level.

In some embodiments, the amplified oligonucleotides comprising cellbarcodes within each partition can be reacted with nucleic acidmolecules attached to macromolecules such as proteins in the partition.The reaction can comprise nucleic acid hybridization between theamplified oligonucleotides and the nucleic acid molecules attached tomacromolecules, and primer extension of a nucleic acid molecule attachedto a macromolecule using an amplified oligonucleotide (which comprises acell barcode or complement thereof) as a template, thereby porting thecell barcode sequence information (and optionally the sample barcodeinformation and/UMI) into the extended nucleic acid molecule attached tothe macromolecule.

In some embodiments, provided herein are methods for generating barcodesand imparting one or more barcodes to the constituent molecules of asingle cell (e.g., constituent molecules in and/or on the single cell).In some embodiments, each single cell in a cell population can belabeled with a unique barcode code (or a unique combination of barcodecodes) that corresponds to the single cell and not another single cellin the population, and the unique barcode codes or combinations thereofcan be referred to as single cell barcodes. Additionally, methods tooverlay sample barcode and spatial barcode information onto the singlecell barcodes are also described. In an exemplary embodiment, thegenomic DNA of a cell is labeled, preferably in situ, with a smallhandful, preferably just a one or two cellular barcode probes (CBP) thatcan be amplified and propagated to label the constituent molecules ofthe cell. In some embodiments, the CBP comprises a Genome BindingSequence (GBS) which targets the CBP probe to a specific locus withinthe genome by virtue of complementary hybridization of the GBS to thetarget locus. In some cases, this GBS sequence can be organism specificand different GBS sequences can be used for different organisms. In someembodiments, a method to enable the attachment of only one or two DNAcellular barcodes to the entire cell comprises tagging the genomic DNA(gDNA) at a single copy locus within the genome using appropriatelydesigned CBP/GBS sequences and/or genome targeting moieties (e.g.,CRISPR/Cas9, TALEs, etc.). In some embodiments, labeling of a singlecopy of a locus can generate two cell barcode probes (CBPs) in a singlecell due to the diploid nature of the genome. In some embodiments, theCBP is designed to be attached to a gDNA locus, so that a single copy ofCBP remains within cells or nuclei after nonspecifically bound CBPs areremoved by washing. This can be achieved by targeting a CBP to a uniquegenomic polymorphism, a mutation site, or a differentially methylatedregion (e.g., attaching CBPs to gDNA in a methylation-specific manner).In some embodiments, the targeting locus of gDNA is not transcribed inorder to prevent interference from transcribed RNA during the CBPannealing and labeling process. In some embodiments, specific targetingemploys specific gDNA-binding enzyme recognition (e.g., CRISPR orTALE-based approaches) of dsDNA, which can also deliver only a singlecopy of CBP to each individual cell or nucleus.

In some embodiments, provided herein is a method for barcodingmacromolecules (e.g., generating macromolecules comprising a barcode)from a sample comprising a population of cells, the method comprisingthe following steps:

a. permeabilizing cells or nuclei, and optionally fixing cells ornuclei, from the population of cells of the sample (dispersed cells,cells within a tissue, etc.);b. optionally making genomic DNA of the permeabilized cells or nuclei atleast partially accessible to nucleic acid hybridization;c. delivering cell barcode probes to the permeabilized cells and/ornuclei of the permeabilized cells, wherein a given cell barcode probecomprises a genome binding element shared among the cell barcode probes,and a cell barcode unique for a given cell barcode probe, and whereinthe genome binding element hybridizes to a region in the genomic DNA,thereby forming a nucleic acid duplex between the genome binding elementand the region of the genomic DNA in the cells and/or nuclei;d. removing cell barcode probes that are not bound to the genomic DNAfrom the cells or nuclei, whereby no more than a defined number ofcopies of the cell barcode probe remain in each cell or nucleus;e. optionally disassociating cells within tissue, and partitioning thecells or nuclei into a plurality of compartments;f. amplifying the cell barcodes within compartments of the plurality ofcompartments, thereby forming amplified cell barcodes within thecompartments;g. attaching the amplified cell barcodes to the macromolecules withinthe compartments, thereby forming barcoded macromolecules.

In another embodiment, provided herein is a method for barcodingmacromolecules from a sample comprising a population of cells, themethod comprising the following steps:

a. permeabilizing cells, or nuclei of the cells, from the population ofcells of the sample;b. delivering reactive primers that are configured to be covalentlyattached to components of the permeabilized cells, thereby creating aplurality of attached primers;c. optionally making genomic DNA of the permeabilized cells or nuclei atleast partially accessible to nucleic acid hybridization;d. delivering cell barcode probes to the permeabilized cells and/ornuclei of the permeabilized cells, wherein a given cell barcode probecomprises a genome binding element shared among the cell barcode probes,and a cell barcode unique for a given cell barcode probe, and whereinthe genome binding element hybridizes to a region in the genomic DNA,thereby forming a nucleic acid duplex between the genome binding elementand the region of the genomic DNA in the cells and/or nuclei;e. removing cell barcode probes that are not bound to the genomic DNAfrom the cells or nuclei, whereby no more than a defined number ofcopies of the cell barcode probe remain in each cell or nucleus;f. amplifying the cell barcodes using the plurality of attached primers,thereby forming amplified cell barcodes within the compartments;g. attaching the amplified cell barcodes to the macromolecules withincells, thereby forming barcoded macromolecules.

In yet another embodiment, provided herein is a method for barcodingmacromolecules from a sample comprising a population of cells, themethod comprising the following steps:

a. permeabilizing cells, or nuclei of the cells, from the population ofcells of the sample;b. delivering a specific genomic DNA-binding carrier comprising a cellbarcode probe to the permeabilized cells or nuclei, wherein a given cellbarcode probe comprises a cell barcode unique for each cell or nucleus,and a priming site, and wherein the specific genomic DNA-binding carrierspecifically binds to a region in the genomic DNA of the cells ornuclei;c. removing specific genomic DNA-binding carriers that are not bound tothe genomic DNA from the cells or nuclei, whereby no more than a definednumber of copies of the cell barcode probe remain in each cell ornucleus;d. amplifying the cell barcodes that were not removed from the cells ornuclei at step (c), thereby forming amplified cell barcodes;e. attaching the amplified cell barcodes to the macromolecules, therebyforming barcoded macromolecules.

These and other aspects or embodiments of the invention will be apparentupon reference to the following detailed description. To this end,various references are set forth herein which describe in more detailcertain background information, procedures, compounds and/orcompositions, and are each hereby incorporated by reference in theirentireties.

BRIEF DESCRIPTION OF THE DRAWINGS

Non-limiting embodiments of the present invention will be described byway of example with reference to the accompanying figures, which areschematic and are not intended to be drawn to scale. For purposes ofillustration, not every component is labeled in every figure, nor isevery component of each embodiment of the invention shown whereillustration is not necessary to allow those of ordinary skill in theart to understand the invention.

FIG. 1 . Exemplary flow diagram for barcoding of macromolecules ofindividual cells showing key steps of the methods disclosed herein.

FIG. 2A-C. Exemplary flow diagrams for single cell multi-omics analysisusing cellular barcoding. FIG. 2A. Exemplary flow diagram for singlecell suspension multi-omics analysis using nuclei cellular barcodetagging and Emulsion PCR (ePCR). The steps in grey can be performed inany order and include protein tagging with DNA recording tag (rTags)stubs, in situ cDNA labeling, nuclear ATAC-Seq labeling, and nuclearlabeling with a cellular barcode probe (CBP). After encoding, the singlecells are partitioned into compartments, and ePCR is used to incorporatethe CBP tag into the ATAC-Seq, RNA-Seq, and/or Prot-Seq DNA tags. Thesepre-library constructs are further processed to prepare scATAC-Seq,scRNA-Seq, and/or scProt-Seq libraries. For short read NGS sequencing ofscRNA-Seq libraries, the cDNA library constructs can use furtherprocessing involving PCR, fragmentation, adapterization using protocolssuch as SMART-Seq (tagmentation; full length), STRT-seq-2i(tagmentation, 5′ end) and SCRB-Seq (tagmentation, 3′ end) (see Lafzi,Atefeh, et al., 2018. “Tutorial: Guidelines for the Experimental Designof Single-Cell RNA Sequencing Studies.” Nature Protocols 13 (12):2742-57). FIG. 2B. Exemplary flow diagram showing similar workflow toFIG. 2A, but for a biological sample such as a tissue sample or adherentcells on a slide, such as spatially arrayed (random or ordered) cells ornuclei. FIG. 2C. Exemplary flow diagram showing workflow for analysis ofa biological sample (e.g., a cell or tissue sample having 2D or 3Dspatial information to be analyzed, such as a tissue slice or spatiallyarrayed cells or nuclei) using solid-phase/bridge PCR or in situ PCR,rather than ePCR.

FIG. 3 . Exemplary design of CBP and coupling of amplified CBP to DNAfragments (see also Example 15).

FIG. 4A-FIG. 4E. Exemplary cellular barcoding via nuclear DNA In SituHybridization (ISH) of cellular barcode probes (CBPs) and emulsion PCR(ePCR).

FIG. 4A. The nuclear gDNA of permeabilized cells or nuclei are labeledwith CBP probes comprised of a Genome Binding Sequence (GBS), forward(CBP_(F)) and reverse (CBP_(R)) priming sites, and internal barcodesequences comprised of an optional spatial barcode (SpBC) sequence and acellular barcode (CBC) sequence using modified ISH protocols. FIG. 4B.After annealing and optionally crosslinking the CBPs to their cognategDNA sequence, analytes (e.g., proteins, etc.) within permeabilizedCBP-tagged cells are covalently labeled with a recording tags (rTags)comprised of a CBP amplification primer F (CBP_(F)) and a universal PCRprimer (U_(F)) sequence; in addition, the rTags attached to proteins,cDNA, or ATAC-Seq elements may also comprise additional barcodeinformation (e.g., sample (SBC), spatial, fraction, etc.) and a uniquemolecular identifier (UMI) for more accurate counting during NGSanalysis. FIG. 4C. Permeabilized cells labeled with nuclear CBPs andproteins labeled with rTag CBP_(F) primers are emulsified together witha PCR mix comprising free CBP_(F) and CBP_(R) primers for amplificationof the CBP barcodes. The CBP_(R) primer is in excess over CBP_(F)primer, enabling the CBP to be ported to the protein analytes taggedwith rTag CBP_(F) primer. FIG. 4D. A permeabilized cell whose proteinsare labeled with the rTag CBP_(F) primer. FIG. 4E. A permeabilized cell,shown after ePCR, whose proteins have had the entire CBP sequencetransferred, via polymerase extension during ePCR, to the labeledproteins (the attached CBP polynucleotide forms an extended recordingtag (extended rTag) to be used in further assays). For the downstreamProteoCode assay, the extended rTags are terminated with a CBP_(R)sequence comprised of a 3′ spacer (Sp) sequence for use in theProteoCode™ assay for encoding via primer extension.

FIG. 5A. Exemplary enzymatic methods for ISH tagging of genomic DNA(gDNA) loci with cellular barcode probes (CBPs). Tagging gDNA withcellular barcodes using a combination of endonuclease digestion andExoIII digestion to generate a localized linear ssDNA region, and InSitu Hybridization (ISH) with a CBP comprised of a Genome BindingSequence (GBS) is shown. Fixed/permeabilized cells are incubated with anendonuclease system (RE, CRISPR-Cas, etc.) which generates either a nickor dsDNA break in the genomic DNA either at restriction enzyme (RE) siteor at a gRNA targeted site (CRISPR-Cas). After endonuclease digestion,the fixed/permeabilized cells are exposed to Exonuclease III (ExoIII)which digests DNA from a 3′ nick, blunt end or 3′ recessed end. Thisdigestion creates a long 5′ single strand overhang which is the targetfor ISH annealing of the GBS portion of a Cellular Barcode Probe (CBP)or a splint adaptor for annealing to a CBP. After annealing, the CBP canbe cross-linked or ligated to the 5′ terminus of the gDNA effectivelytagging the gDNA with a CBP.

An exemplar restriction enzyme (RE) digestion can be a PmeI digestion,which cuts on average, every 65,000 bp (8-cutter). ExoIII chews dsDNAback at the 3′ ends. CBP is annealed and ligated onto the target gDNAsequence corresponding to the GBS sequence.

FIG. 5B. Exemplary RecA-coated strand invasion probe for ISH tagging ofgDNA with CBPs.

Fixed/permeabilized cells are incubated with an endonuclease system (RE,CRISPR-Cas, etc.) which generates either a nick or dsDNA break in thegenomic DNA either semi-randomly (RE) or site-specifically (CRISPR-Cas).After endonuclease digestion, the genomic DNA of fixed/permeabilizedcells is annealed with RecA-coated CBP splint adapter enabling ligationof the CBP to the 5′ terminus of the gDNA effectively tagging the gDNAwith a CBP.

FIG. 6 . Exemplary design and use of the padlock CBP in the disclosedbarcoding methods (adopted from Matsunaga and Matsunaga, 2017, “FISHwith Padlock Probes Can Efficiently Reveal the Genomic Position of Lowor Single-Copy DNA Sequences.” Cytologia 82 (4): 337-39; Yaroslavsky andSmolina, 2013).

FIG. 7A-FIG. 7C. Exemplary designs of Cellular Barcode Probe (CBP) andtransfers CBP to macromolecules within individual cell.

FIG. 7A. The CBP is comprised of several functional sequence elements.The Genome Binding Sequence (GBS), which anneals to a target locus(preferably, unique) on the gDNA of the cell, the CBP forwardamplification primer (CBP_(F)), an optional Sample or Spatial Barcode(SBC or SpBC), the Cellular Barcode (CBC), and the CBP reverse primer(CBP_(R)). During amplification, both forward and reverse strands of theCBP (minus the GBS sequence) are generated. The reverse copies of theCBP amplicons diffuse throughout the cell and anneal to the rTag primersequences attached to the macromolecules (e.g., proteins, cDNA, etc.)and the CBP information is copied to the rTags during the amplificationreaction. The final result is CBP-tagged macromolecules with acell-specific barcode. The rTag can comprise the CBP_(F) on the 3′ endand optionally comprise the SBC, UMI, U_(F) (e.g., as shown in FIG. 4B)and other elements on the 5′ of the CBP_(F). The CBP_(F) in the rTag canhybridize to the CBP′_(F) (complement of the CBP) and port the CBC andoptionally SBC information into the rTag.

FIG. 7B. Proteins within a permeabilized cell are labeled with DNArecording tag stubs (rTags) using a two-step reaction, in which thefirst step uses a heterobifunctional linker for activation of lysines onthe proteins converting the amines to a click chemistry moiety (e.g.,TCO), which in a subsequent step is coupled to an rTag bearing an mTetmoiety, which reacts via iEDDA bioconjugation chemistry to theTCO-derivitized proteins.

FIG. 7C. CBP tagging of cDNA within the cell using a modifiedSTRT-seq-2i protocol for 5′ RNA-seq tag counting. During reversetranscription of mRNA into cDNA, an oligo dT primer comprised of auniversal PCR sequence (PCR_(F)) anneals to the polyA sequence on themRNA and generates a 1^(st) cDNA strand incorporating the CBP′_(F)sequence. Using a SMART cDNA protocol employing template switchingreverse transcription and template switch oligo primer (TSO) containinga universal priming site (U_(TSO)) and 3′ GGG nucleotides (orribonucleotides, or LNA), enables completion of the 1^(st) strand with aflanking 3‘ CBP’F sequence and a TSO sequence. During CBP amplification,the 2^(nd) strand primes on the CBP copy strand and effectively transferCBP information to the 2^(nd) strand DNA sequence. An NGS library iscreated from this product by amplifying with the PCR primers, PCR_(F)and CBP_(R). A short read NGS library is created from this PCR productby a tagmentation reaction coupled with a second and PCR amplificationreaction using the tagmentation primer and CBP_(R) to enable 5′ RNA-Seqtag counting.

FIG. 7D. CBP tagging of cDNA within the cell using a modified SCRB-seqprotocol for 3′ RNA-Seq tag counting (Soumillon, et al., 2014.“Characterization of Directed Differentiation by High-ThroughputSingle-Cell RNA-Seq.” bioRxiv). SCRB-Seq relies on a template-switchingreverse transcriptase to convert poly(A)+mRNA from isolated single cellsto cDNA decorated with universal adapters, single cell barcodes andunique molecular identifiers (UMIs). During reverse transcription ofmRNA into cDNA, an oligo dT primer containing a 5′CBP′_(F) anneals tothe polyA sequence on the mRNA and generates a 1^(st) cDNA strandincorporating the CBP′_(F) sequence. Using a SMART-Seq or SCRB-Seq cDNAprotocol employing template switching reverse transcription and templateswitch oligo (TSO) containing a universal priming site and a 3′ Gnucleotides (or ribonucleotides, LNA), enables completion of the 1^(st)strand with a flanking 3′ CBP′_(F) sequence and a PCR amplificationsequence. During CBP amplification, the 2^(nd) strand primes on the CBPcopy strand and effectively transfers CBP information to the 2^(nd)strand DNA sequence. An NGS library is created from this product byamplifying with the TSO PCR_(F) primer and the CBP_(R) primer. A shortread NGS library is created from this PCR product by a tagmentationreaction coupled with a second and PCR amplification reaction using thetagmentation primer and CBP_(R) to enable 3′ RNA-Seq tag counting.

FIG. 8A-FIG. 8C. Exemplary designs of specific genomic DNA-bindingcarriers (CRISPR-dCas9) for locus-specific targeting of Cellular BarcodeProbes (CBPs).

FIG. 8A. The CBP probe (RNA) is contiguous with a portion of thegRNA/tracRNA of the ribonucleotide dCas9 complex, or, in FIG. 8B, the CBprobe (DNA) is annealed to a complementary region of the gRNA/tracRNA.In the case of an RNA CBP probe, reverse transcription is used to writeit into a DNA sequence. FIG. 8C. Alternatively, the CBP can becovalently attached to the dCas9 via a fusion construct; in the exampleshown, the dCas9 is fused to a SpyCatcher (SpyC) protein whichcovalently binds a SpyTag (SpyT) peptide coupled to a DNA CBP sequence.

FIG. 9A-FIG. 9C. Exemplary prime editing in permeabilized cells toattach cellular barcode probes.

FIG. 9A. A nicking Cas9 (non-target strand cleavage) is loaded with aprime editing guide RNA (pegRNA) which is comprised of a 3′ portionencompassing the cellular barcode probe and a complementary region tothe targeted DNA (genome-binding region). FIG. 9B. Nicking of thenon-target strand with nCas9 creates a 3′ ssDNA terminus that extends onthe pegRNA terminus through action of a Reverse Transcriptase (RT). FIG.9C. This step effectively writes the CBP into the gDNA for downstreamsingle cell barcoding applications.

FIG. 10 . Exemplary site-specific cellular barcode tagging of imprintedloci. An adenine base labeled with a bipyridyl moiety chelates osmiumtetroxide and covalently attaches to opposing methyl cytosine bases.Adapted from Buchmuller, et al., 2021. “Programmable Tools for TargetedAnalysis of Epigenetic DNA Modifications.” Current Opinion in ChemicalBiology 63 (August): 1-10.

FIG. 11A-FIG. 11B. Exemplary in silico merging macromolecules from thesame droplet barcoded by two or more barcode sequences. FIG. 11A. UniqueMolecular Identifier (UMI) sequences incorporated in the macromolecules,such as cell DNA fragments, are used. The cell barcodes from the samedroplet will share UMI sequences at a rate exceeding what may beexpected by chance. For each pair of cell barcodes, the Jaccard index iscomputed over the UMI sequences, providing a measure of how similar theUMI sequences are for any pair of cell barcodes. FIG. 11B. From thesepairwise Jaccard index statistics, a knee plot is generated to determinepairs that are likely to have originated from the same droplet, and aJaccard index cutoff value is used to determine barcode pairs that needto be merged.

FIG. 12 . Exemplary method of hydrogelation of fixed/permeabilized cellsfor templated emulsions. Fixed/permeabilized cells are labeled with CBPand rTags as described in Example 2. Then, the cells are infused with acleavable polymer mix (PEGSSDA), a photo-activated crosslinking agent,and primers and PCR mix. Exposure to UV 365 nm light source ofappropriate intensity cross-links the polymer forming hydrogel withinthe interior of the cell. The hydrogelated cell is durable and serves asa particle in templated emulsion formation. Then, the hydrogel isdissolved by exposing the encapsulated cell to a reducing agent such asdithiothreitol (DTT) in saturated fluoropolymer oil. Finally, the cellis ready for emulsion PCR (ePCR). Adopted from Li, Siran, et al., 2020.“Copolymerization of Single-Cell Nucleic Acids into Balls of AcrylamideGel.” Genome Research 30 (1): 49-61.

FIG. 13 illustrates exemplary generation of compartment barcoded nucleicacid recording tags attached to peptides. Compartment barcodingtechnology (e.g., barcoded beads in microfluidic droplets, etc.) can beused to transfer a compartment-specific barcode to molecular contentsencapsulated within a particular compartment. In a particularembodiment, the protein molecule is denatured, and the F-amine group oflysine residues (K) is chemically conjugated to an activated universalDNA tag molecule (comprising a universal priming sequence (U1)), shownwith NHS moiety at the 5′ end). After conjugation of universal DNA tagsto the polypeptide, excess universal DNA tags are removed. Then, theuniversal DNA tagged polypeptides are hybridized to nucleic acidmolecules bound to beads, wherein the nucleic acid molecules bound to anindividual bead comprise a unique population of compartment tag(barcode) sequences. The compartmentalization can occur by separatingthe sample into different physical compartments, such as droplets(illustrated by the dashed oval). Alternatively, compartmentalizationcan be directly accomplished by the immobilization of the labeledpolypeptides on the bead surface, e.g., via annealing of the universalDNA tags on the polypeptide to the compartment DNA tags on the bead,without the need for additional physical separation. A singlepolypeptide molecule interacts with only a single bead (e.g., a singlepolypeptide does not span multiple beads). Multiple polypeptides,however, may interact with the same bead. In addition to the compartmentbarcode sequence (BC), the nucleic acid molecules bound to the bead maybe comprised of a common Sp (spacer) sequence, a unique molecularidentifier (UMI), and a sequence complementary to the polypeptide DNAtag, U1′. After annealing of the universal DNA tagged polypeptides tothe compartment tags bound to the bead, the compartment tags arereleased from the beads via cleavage of the attachment linkers.

FIG. 14 . Exemplary compartmentalization of cells in droplets.Individual cells or nuclei having CBPs are partitioning into a pluralityof compartments by droplet formation through a T-junction microfluidicor flow focusing device. In the Y or T-junction shown, one aqueous flowstream contains the cell lysis detergent (e.g., LiDS lysis buffer: 100mM Tris pH 7.5, 500 mM LiCl, 10 mM EDTA, 1% lithium dodecyl sulfate, 5mM DTT) and PCR mix and the other aqueous flow stream contains thesuspended cells in an isotonic buffer (e.g., PBS). The detergent can bean ionic (e.g., SDS, LDS, etc.), non-ionic (e.g., TX-100, Tween-20,etc.), or zwitterionic (e.g., CHAPS, CHAPSO). Moreover, duringemulsification and droplet formation, the droplet interior, such as pH,presence of a reducing agent, activatable detergent, etc., can bemodified by addition of a reagent to the fluoro-oil of the emulsion.

FIG. 15 . Exemplary compartmentalization of individual cells indroplets, followed by cell barcode amplification, transfer barcodeinformation to rTags of protein analytes and NGPA assay for the taggedprotein analytes. (A) Single cells are fixed, permeabilized, and havetheir nuclei labeled with CBPs. (B) Single cells are encapsulated indroplets along with a polymerizable matrix and lysis buffer. (C) Polymermatrix polymerizes and immobilizes DNA rTags within matrix. (D) Proteinsreleased from the cell conjugate to activated DNA rTags within polymermatrix. (E) Single cell polymer beads (SCPB) are extracted into aqueousphase and combinatorial barcodes can be added to SCPBs via a SCI-Seqsplit-pool process. (F) The resultant SCPBs can be used directly in aProteoCode NGPA immunoassay (exemplary antibody readout shown) orprocessed for an NGPS assay for quantitative assessment of proteins fromsingle cell.

Approaches for compartmental-based partitioning include dropletformation through microfluidic devices using T-junctions and flowfocusing, emulsion generation using agitation or extrusion through amembrane with small holes (e.g., track etch membrane), and others.

FIG. 16A-FIG. 16B. Exemplary “bridge” amplification of a cell barcodeprobe using a pair of primers attached to porous sepharose beads. FIG.16A. Design of “bridge” amplification. FIG. 16B. Exemplary results ofon-bead “bridge” amplification show amplified product quantificationusing variable P5/P7 primer density.

DETAILED DESCRIPTION

Numerous specific details are set forth in the following description inorder to provide a thorough understanding of the present disclosure.These details are provided for the purpose of example and the claimedsubject matter may be practiced according to the claims without some orall of these specific details. It is to be understood that otherembodiments can be used and structural changes can be made withoutdeparting from the scope of the claimed subject matter. It should beunderstood that the various features and functionality described in oneor more of the individual embodiments are not limited in theirapplicability to the particular embodiment with which they aredescribed. They instead can be applied, alone or in some combination, toone or more of the other embodiments of the disclosure, whether or notsuch embodiments are described, and whether or not such features arepresented as being a part of a described embodiment. For the purpose ofclarity, technical material that is known in the technical fieldsrelated to the claimed subject matter has not been described in detailso that the claimed subject matter is not unnecessarily obscured.

All publications, including patent documents, scientific articles anddatabases, referred to in this application are incorporated by referencein their entireties for all purposes to the same extent as if eachindividual publication were individually incorporated by reference.Citation of the publications or documents is not intended as anadmission that any of them is pertinent prior art, nor does itconstitute any admission as to the contents or date of thesepublications or documents.

All headings are for the convenience of the reader and should not beused to limit the meaning of the text that follows the heading, unlessso specified.

Definitions

Unless defined otherwise, all technical and scientific terms used hereinhave the same meaning as is commonly understood by one of ordinary skillin the art to which the present disclosure belongs. If a definition setforth in this section is contrary to or otherwise inconsistent with adefinition set forth in the patents, applications, publishedapplications and other publications that are herein incorporated byreference, the definition set forth in this section prevails over thedefinition that is incorporated herein by reference. Unless the contextrequires otherwise, throughout the specification and claims whichfollow, the word “comprise” and variations thereof, such as, “comprises”and “comprising,” are to be construed in an open, inclusive sense, thatis, as “including, but not limited to.”

Reference throughout this specification to “one embodiment” or “anembodiment” means that a particular feature, structure or characteristicdescribed in connection with the embodiment is included in at least oneembodiment. Thus, the appearances of the phrases “in one embodiment” or“in an embodiment” in various places throughout this specification arenot necessarily all referring to the same embodiment. Furthermore, theparticular features, structures, or characteristics may be combined inany suitable manner in one or more embodiments.

As used herein, the singular forms “a,” “an” and “the” include pluralreferents unless the context clearly dictates otherwise. Thus, forexample, reference to “a peptide” includes one or more peptides, ormixtures of peptides. Also, and unless specifically stated or obviousfrom context, as used herein, the term “or” is understood to beinclusive and covers both “or” and “and”.

The term “about” as used herein refers to the usual error range for therespective value readily known to the skilled person in this technicalfield. Reference to “about” a value or parameter herein includes (anddescribes) embodiments that are directed to that value or parameter perse. For example, description referring to “about X” includes descriptionof “X.

The term “antibody” herein is used in the broadest sense and includespolyclonal and monoclonal antibodies, including intact antibodies andfunctional (antigen-binding) antibody fragments, including fragmentantigen binding (Fab) fragments, F(ab′)₂ fragments, Fab′ fragments, Fvfragments, recombinant IgG (rIgG) fragments, single chain antibodyfragments, including single chain variable fragments (scFv), and singledomain antibodies (e.g., sdAb, sdFv, nanobody) fragments. The termencompasses genetically engineered and/or otherwise modified forms ofimmunoglobulins, such as intrabodies, peptibodies, chimeric antibodies,fully human antibodies, humanized antibodies, and heteroconjugateantibodies, multispecific, e.g., bispecific, antibodies, diabodies,tandem di-scFv, tandem tri-scFv. Unless otherwise stated, the term“antibody” should be understood to encompass functional antibodyfragments thereof. The term also encompasses intact or full-lengthantibodies, including antibodies of any class or sub-class, includingIgG and sub-classes thereof, IgM, IgE, IgA, and IgD.

As used herein, the term “sample” refers to anything which may containan analyte for which an analyte assay is desired. As used herein, a“sample” can be a solution, a suspension, liquid, powder, a paste,aqueous, non-aqueous or any combination thereof. In some embodiments,the sample is a biological sample. A biological sample of the presentdisclosure encompasses a sample in the form of a solution, a suspension,a liquid, a powder, a paste, an aqueous sample, or a non-aqueous sample.As used herein, a “biological sample” includes any sample obtained froma living or viral (or prion) source or other source of macromoleculesand biomolecules, and includes any cell type or tissue of a subject fromwhich nucleic acid, protein and/or other macromolecule can be obtained.The biological sample can be a sample obtained directly from abiological source or a sample that is processed. For example, isolatednucleic acids that are amplified constitute a biological sample.Biological samples include, but are not limited to, body fluids, such asblood, plasma, serum, cerebrospinal fluid, synovial fluid, urine andsweat, tissue and organ samples from animals and plants and processedsamples derived therefrom. A biological sample may also be comprised ofa tissue biopsy such as tissue section, a slide-mounted tissue section,an enriched fraction of cells of interest, etc.

The terms “level” or “levels” are used to refer to the presence and/oramount of a target, e.g., a substance or an organism that is part of theetiology of a disease or disorder, and can be determined qualitativelyor quantitatively. A “qualitative” change in the target level refers tothe appearance or disappearance of a target that is not detectable or ispresent in samples obtained from normal controls. A “quantitative”change in the levels of one or more targets refers to a measurableincrease or decrease in the target levels when compared to a healthycontrol.

As used herein, the term “macromolecule” encompasses large moleculescomposed of smaller subunits. Examples of macromolecules include, butare not limited to peptides, polypeptides, proteins, nucleic acids,carbohydrates, lipids, macrocycles, or a combination or complex thereof.A macromolecule also includes a chimeric macromolecule composed of acombination of two or more types of macromolecules, covalently linkedtogether (e.g., a peptide linked to a nucleic acid). A macromolecule mayalso include a “macromolecule assembly”, which is composed ofnon-covalent complexes of two or more macromolecules. A macromoleculeassembly may be composed of the same type of macromolecule (e.g.,protein-protein) or of two or more different types of macromolecules(e.g., protein-DNA).

As used herein, the term “polypeptide” is used interchangeably with theterm “peptide” refers to a molecule comprising a chain of two or moreamino acid residues joined by peptide bonds. In some embodiments, apolypeptide comprises 2 to 50 amino acids. In some embodiments, apolypeptide does not comprise a secondary, tertiary, or higherstructure. In some embodiments, the polypeptide is a protein. In someembodiments, a polypeptide comprises more than 50 amino acid residues.In some embodiments, in addition to a primary structure, a polypeptidecomprises a secondary, tertiary, or higher structure. The amino acids ofthe polypeptides are most typically L-amino acids, but may also beD-amino acids, modified amino acids, amino acid analogs, amino acidmimetics, or any combination thereof. Polypeptides can be naturallyoccurring, synthetically produced, recombinantly expressed, isolated, orbe produced by a combination of the described methodologies.Polypeptides may also comprise additional groups modifying the aminoacid chain, for example, functional groups added via post-translationalmodification. The polypeptide macromolecule may be linear or branched,it may comprise modified amino acids, and it may be interrupted bynon-amino acids. The term also encompasses an amino acid polymer thathas been modified naturally or by intervention; for example, disulfidebond formation, glycosylation, lipidation, acetylation, phosphorylation,or any other manipulation or modification, such as conjugation with alabeling component.

As used herein, the term “amino acid” refers to an organic compoundcomprising an amine group, a carboxylic acid group, and a side-chainspecific to each amino acid, which serve as a monomeric subunit of apeptide. An amino acid includes the 20 standard, naturally occurring orcanonical amino acids as well as non-standard amino acids. The standard,naturally-occurring (or natural) amino acids include Alanine (A or Ala),Cysteine (C or Cys), Aspartic Acid (D or Asp), Glutamic Acid (E or Glu),Phenylalanine (F or Phe), Glycine (G or Gly), Histidine (H or His),Isoleucine (I or Ile), Lysine (K or Lys), Leucine (L or Leu), Methionine(M or Met), Asparagine (N or Asn), Proline (P or Pro), Glutamine (Q orGln), Arginine (R or Arg), Serine (S or Ser), Threonine (T or Thr),Valine (V or Val), Tryptophan (W or Trp), and Tyrosine (Y or Tyr). Anamino acid may be an L-amino acid or a D-amino acid. Non-standard aminoacids may be modified amino acids, amino acid analogs, amino acidmimetics, non-standard proteinogenic amino acids, or non-proteinogenicamino acids that occur naturally or are chemically synthesized. Examplesof non-standard amino acids include, but are not limited to,selenocysteine, pyrrolysine, and N-formylmethionine, R-amino acids,Homo-amino acids, Proline and Pyruvic acid derivatives, 3-substitutedalanine derivatives, glycine derivatives, ring-substituted phenylalanineand tyrosine derivatives, linear core amino acids, N-methyl amino acids.The term “amino acid residue” refers to an amino acid incorporated intoa polypeptide that forms peptide bond(s) with neighboring amino acid(s).

As used herein, the term “post-translational modification” refers tomodifications that occur on a peptide after its translation, e.g.,translation by ribosomes, is complete. A post-translational modificationmay be a covalent chemical modification or enzymatic modification.Examples of post-translation modifications include, but are not limitedto, acylation, acetylation, alkylation (including methylation),biotinylation, butyrylation, carbamylation, carbonylation, deamidation,deiminiation, diphthamide formation, disulfide bridge formation,eliminylation, flavin attachment, formylation, gamma-carboxylation,glutamylation, glycylation, glycosylation, glypiation, heme Cattachment, hydroxylation, hypusine formation, iodination,isoprenylation, lipidation, lipoylation, malonylation, methylation,myristolylation, oxidation, palmitoylation, pegylation,phosphopantetheinylation, phosphorylation, prenylation, propionylation,retinylidene Schiff base formation, S-glutathionylation,S-nitrosylation, S-sulfenylation, selenation, succinylation,sulfination, ubiquitination, and C-terminal amidation. Apost-translational modification includes modifications of the aminoterminus and/or the carboxyl terminus of a peptide. Modifications of theterminal amino group include, but are not limited to, des-amino, N-loweralkyl, N-di-lower alkyl, and N-acyl modifications. Modifications of theterminal carboxy group include, but are not limited to, amide, loweralkyl amide, dialkyl amide, and lower alkyl ester modifications (e.g.,wherein lower alkyl is C₁-C₄ alkyl). A post-translational modificationalso includes modifications, such as but not limited to those describedabove, of amino acids falling between the amino and carboxy termini. Theterm post-translational modification can also include peptidemodifications that include one or more detectable labels.

The term “detectable label” as used herein refers to a substance whichcan indicate the presence of another substance when associated with it.The detectable label can be a substance that is linked to orincorporated into the substance to be detected. In some embodiments, adetectable label is suitable for allowing for detection and alsoquantification, for example, a detectable label that emitting adetectable and measurable signal. Examples of detectable labels includea dye, a fluorophore, a chromophore, a fluorescent nanoparticle (e.g.quantum dot), a radiolabel, an enzyme (e.g. alkaline phosphatase,luciferase or horseradish peroxidase), or a chemiluminescent orbioluminescent molecule.

As used herein, the term “linker” refers to one or more of a nucleotide,a nucleotide analog, an amino acid, a peptide, a polypeptide, a polymer,or a non-nucleotide chemical moiety that is used to join two molecules.A linker may be used to join a recording tag with a polypeptide, apolypeptide with a solid support, a recording tag with a solid support,etc. In certain embodiments, a linker joins two molecules via enzymaticreaction or chemistry reaction (e.g., a click chemistry reaction).

The term “ligand” as used herein refers to any molecule or moietyconnected to the compounds described herein. “Ligand” may refer to oneor more ligands attached to a compound. In some embodiments, the ligandis a pendant group or binding site (e.g., the site to which the bindingagent binds).

As used herein, the term “barcode” refers to a nucleic acid molecule ofabout 3 to about 30 bases (e.g., 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13,14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29 or 30bases) providing a unique identifier tag or origin information for apolypeptide, a binding agent, a set of binding agents from a bindingcycle, a sample polypeptides, a set of samples, polypeptides within acompartment (e.g., droplet, bead, or separated location), polypeptideswithin a set of compartments, a fraction of polypeptides, a set ofpolypeptide fractions, a spatial region or set of spatial regions, alibrary of polypeptides, or a library of binding agents. A barcode canbe an artificial sequence or a naturally occurring sequence. In certainembodiments, each barcode within a population of barcodes is different.In other embodiments, a portion of barcodes in a population of barcodesis different, e.g., at least about 10%, 15%, 20%, 25%, 30%, 35%, 40%,45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 97%, or 99% ofthe barcodes in a population of barcodes is different. A population ofbarcodes may be randomly generated or non-randomly generated. In certainembodiments, a population of barcodes are error-correcting orerror-tolerant barcodes. Barcodes can be used to computationallydeconvolute the multiplexed sequencing data and identify sequence readsderived from an individual polypeptide, sample, library, etc. A barcodecan also be used for deconvolution of a collection of polypeptides thathave been distributed into small compartments for enhanced mapping.

A “sample barcode”, also referred to as “sample tag” identifies fromwhich sample a macromolecule derives.

A “spatial barcode” which region of a 2-D or 3-D tissue section fromwhich a macromolecule derives. Spatial barcodes may be used formolecular pathology on tissue sections. A spatial barcode allows formultiplex sequencing of a plurality of samples or libraries from tissuesection(s).

As used herein, the term “solid support”, or “substrate” refers to anysolid material, including porous and non-porous materials, to which amacromolecule can be associated directly or indirectly, by any meansknown in the art, including covalent and non-covalent interactions, orany combination thereof. A solid support may be two-dimensional (e.g.,planar surface) or three-dimensional (e.g., gel matrix or bead). A solidsupport can be any support surface including, but not limited to, abead, a microbead, an array, a glass surface, a silicon surface, aplastic surface, a filter, a membrane, a PTFE membrane, a silicon waferchip, a flow through chip, a flow cell, a biochip including signaltransducing electronics, a channel, a microtiter well, an ELISA plate, aspinning interferometry disc, a nitrocellulose-based polymer surface, apolymer matrix, a nanoparticle, or a microsphere. Materials for a solidsupport include but are not limited to acrylamide, agarose, cellulose,dextran, nitrocellulose, glass, gold, quartz, polystyrene, polyethylenevinyl acetate, polypropylene, polyester, polymethacrylate, polyacrylate,polyethylene, polyethylene oxide, polysilicates, polycarbonates, polyvinyl alcohol (PVA), Teflon, fluorocarbons, nylon, silicon rubber,polyanhydrides, polyglycolic acid, polyvinylchloride, polylactic acid,polyorthoesters, functionalized silane, polypropylfumerate, collagen,glycosaminoglycans, polyamino acids, dextran, or any combinationthereof. For example, when solid surface is a bead, the bead caninclude, but is not limited to, a ceramic bead, a polystyrene bead, apolymer bead, a polyacrylate bead, a methylstyrene bead, an agarosebead, a cellulose bead, a dextran bead, an acrylamide bead, a porousbead, a paramagnetic bead, a glass bead, a controlled pore bead, asilica-based bead, or any combinations thereof. A bead may be sphericalor an irregularly shaped. In certain embodiments, beads range in sizefrom about 0.2 micron to about 200 microns, or from about 0.5 micron toabout 5 micron. In some embodiments, beads can be about 1, 1.5, 2, 3, 4,5, 6, 7, 8, 9, 10, 15, or 20 μm in diameter. In certain embodiments, “abead” solid support may refer to an individual bead or a plurality ofbeads. In some embodiments, the solid support is a nanoparticle. Incertain embodiments, the nanoparticles range in size from about 1 nm toabout 500 nm in diameter, for example, between about 1 nm and about 20nm, between about 1 nm and about 50 nm, between about 1 nm and about 100nm, between about 10 nm and about 50 nm, between about 10 nm and about100 nm, between about 10 nm and about 200 nm, between about 50 nm andabout 100 nm, between about 50 nm and about 150, between about 50 nm andabout 200 nm, or between about 200 nm and about 500 nm in diameter.

As used herein, the term “nucleic acid molecule” or “polynucleotide”refers to a single- or double-stranded polynucleotide containingdeoxyribonucleotides or ribonucleotides that are linked by 3′-5′phosphodiester bonds, as well as polynucleotide analogs. A nucleic acidmolecule includes, but is not limited to, DNA, RNA, and cDNA. Apolynucleotide analog may possess a backbone other than a standardphosphodiester linkage found in natural polynucleotides and, optionally,a modified sugar moiety or moieties other than ribose or deoxyribose.Polynucleotide analogs contain bases capable of hydrogen bonding byWatson-Crick base pairing to standard polynucleotide bases, where theanalog backbone presents the bases in a manner to permit such hydrogenbonding in a sequence-specific fashion between the oligonucleotideanalog molecule and bases in a standard polynucleotide. Examples ofpolynucleotide analogs include, but are not limited to xeno nucleic acid(XNA), bridged nucleic acid (BNA), glycol nucleic acid (GNA), peptidenucleic acids (PNAs), morpholino polynucleotides, locked nucleic acids(LNAs), threose nucleic acid (TNA), 2′-O-Methyl polynucleotides,2′-O-alkyl ribosyl substituted polynucleotides, phosphorothioatepolynucleotides, and boronophosphate polynucleotides. A polynucleotideanalog may possess purine or pyrimidine analogs, including for example,7-deaza purine analogs, 8-halopurine analogs, 5-halopyrimidine analogs,or universal base analogs that can pair with any base, includinghypoxanthine, nitroazoles, isocarbostyril analogues, azole carboxamides,and aromatic triazole analogues, or base analogs with additionalfunctionality, such as a biotin moiety for affinity binding. In someembodiments, the nucleic acid molecule or oligonucleotide is a modifiedoligonucleotide. In some embodiments, the nucleic acid molecule oroligonucleotide is a DNA with pseudo-complementary bases, a DNA withprotected bases, an RNA molecule, a BNA molecule, an XNA molecule, a LNAmolecule, a PNA molecule, or a morpholino DNA, or a combination thereof.In some embodiments, the nucleic acid molecule or oligonucleotide isbackbone modified, sugar modified, or nucleobase modified. In someembodiments, the nucleic acid molecule or oligonucleotide has nucleobaseprotecting groups such as Alloc, electrophilic protecting groups such asthiranes, acetyl protecting groups, nitrobenzyl protecting groups,sulfonate protecting groups, or traditional base-labile protectinggroups.

As used herein, “nucleic acid sequencing” means the determination of theorder of nucleotides in a nucleic acid molecule or a sample of nucleicacid molecules. Similarly, “polypeptide sequencing” means thedetermination of the identity and order of at least a portion of aminoacids in the polypeptide molecule or in a sample of polypeptidemolecules.

As used herein, “analyzing” the macromolecule refers to identify,detect, quantify, characterize, distinguish, or a combination thereof,all or a portion of the components of the macromolecule. For example,analyzing a polypeptide includes determining all or a portion of theamino acid sequence (contiguous or non-continuous) of the polypeptide.Analyzing a polypeptide also includes partial identification of acomponent of the polypeptide.

As used herein “amplification” refers to any in vitro method forincreasing the number of copies of a nucleotide sequence with the use ofa DNA polymerase. Nucleic acid amplification results in theincorporation of nucleotides into a DNA molecule or primer therebyforming a new DNA molecule complementary to a DNA template. The formedDNA molecule and its template can be used as templates to synthesizeadditional DNA molecules.

The terms “hybridization” and “hybridizing” refers to the pairing of twocomplementary single-stranded nucleic acid molecules (RNA and/or DNA) toform a double-stranded molecule (nucleic acid duplex). As used herein,two nucleic acid molecules may be hybridized, although the base pairingis not completely complementary. Accordingly, mismatched bases do notprevent hybridization of two nucleic acid molecules provided thatappropriate conditions, well known in the art, are used. In the presentinvention, the term “hybridization” refers particularly to hybridizationof an oligonucleotide to a template molecule.

As used herein, the term “primer extension”, also referred to as“polymerase extension”, refers to a reaction catalyzed by a nucleic acidpolymerase (e.g., DNA polymerase) whereby a nucleic acid molecule (e.g.,oligonucleotide primer, spacer sequence) that anneals to a complementarystrand is extended by the polymerase, using the complementary strand astemplate.

As used herein, the term “recording tag” and term “coding tag” refer toa nucleic acid molecule or sequenceable polymer molecule (see, e.g., Niuet al., 2013, Nat. Chem. 5:282-292) that optionally comprisesidentifying information for a macromolecule to which it is associated. Arecoding tag or coding tag may be directly linked to a macromolecule,linked to a macromolecule via a multifunctional linker, or associatedwith a macromolecule by virtue of its proximity (or co-localization) ona solid support. A recording tag or coding tag may further compriseother functional components, e.g., a universal priming site, uniquemolecular identifier, a barcode (e.g., a sample barcode, a fractionbarcode, spatial barcode, a compartment tag, etc.), a spacer sequencethat is complementary to a spacer sequence of a coding tag, or anycombination thereof.

As used herein, the term “binding agent” refers to a nucleic acidmolecule, a polypeptide, a carbohydrate, or a small molecule that bindsto, associates, unites with, recognizes, or combines with a bindingtarget, e.g., a macromolecule analyte or a component or feature of amacromolecule analyte. In some embodiments, a binding agent comprises apolypeptide. In some embodiments, a binding agent comprises an aptamer.In some embodiments, a binding agent does not comprise a polynucleotide.In some embodiments, a binding agent form a covalent association withthe macromolecule analyte or component or feature of a macromoleculeanalyte. In other embodiments, a binding agent form a non-covalentassociation with the macromolecule analyte or component or feature of amacromolecule analyte. A binding agent may also be a chimeric bindingagent, composed of two or more types of molecules. A binding agent maypreferably bind to a chemically functionalized or modified amino acid(e.g., an amino acid that has been functionalized or modified by afunctionalizing reagent) over a non-modified amino acid. For example, abinding agent may preferably bind to an amino acid that has beenfunctionalized or modified over an amino acid that is unmodified. Abinding agent may exhibit selective binding to a component or feature ofa polypeptide (e.g., a binding agent may selectively bind to one of the20 possible natural amino acid residues and bind with very low affinityor not at all to the other 19 natural amino acid residues). A bindingagent may exhibit less selective binding, where the binding agent iscapable of binding or configured to bind to a plurality of components orfeatures of a polypeptide (e.g., a binding agent may bind with similaraffinity to two or more different amino acid residues).

The terms “specific binding” generally refers to an engineered bindingagent that binds to a particular functionalized amino acid residue morereadily than it would bind to a random functionalized amino acid residue(e.g., there is a detectable relative increase in the binding of thebinding agent to a specific or group of functionalized amino acidresidues). The term “specificity” is used herein to qualify the relativeaffinity by which an engineered binding agent binds to a cognatefunctionalized amino acid residue. Specific binding typically means thatan engineered binding agent binds to a cognate functionalized amino acidresidue at least twice more likely that to a random, non-cognatefunctionalized amino acid residue (a 2:1 ratio of specific tonon-specific binding). Non-specific binding refers to backgroundbinding, and is the amount of signal that is produced in a binding assaybetween an engineered binding agent and a non-cognate amino acid residueimmobilized on a solid support. In some embodiments, specific bindingrefers to binding between an engineered binding agent and a cognatefunctionalized amino acid residue with a dissociation constant (Kd) of500 nM or less.

Methods for Generating Barcoded Macromolecules from Single Cells.

Provided herein is a method for barcoding macromolecules from a samplecomprising a population of cells, the method comprising the followingsteps:

-   -   a. permeabilizing and optionally fixing cells, or nuclei of the        cells, from the population of cells of the sample;    -   b. optionally making genomic DNA of the permeabilized cells or        nuclei at least partially accessible to nucleic acid        hybridization;    -   c. delivering cell barcode probes to the permeabilized cells        and/or nuclei of the permeabilized cells, wherein a given cell        barcode probe comprises a genome binding element shared among        the cell barcode probes, and a cell barcode unique for a given        cell barcode probe, and wherein the genome binding element        hybridizes to a region in the genomic DNA, thereby forming a        nucleic acid duplex between the genome binding element and the        region of the genomic DNA in the cells and/or nuclei;    -   d. removing cell barcode probes that are not bound to the        genomic DNA from the cells or nuclei, whereby no more than a        defined number of copies of the cell barcode probe remain in        each cell or nucleus;    -   e. partitioning the cells or nuclei into a plurality of        compartments;    -   f. amplifying the cell barcodes within compartments of the        plurality of compartments, thereby forming amplified cell        barcodes within the compartments; and    -   g. attaching the amplified cell barcodes to the macromolecules        within the compartments, thereby forming barcoded        macromolecules.

In another embodiment, provided herein is a method for barcodingmacromolecules from a sample comprising a population of cells, themethod comprising the following steps:

a. permeabilizing cells, or nuclei of the cells, from the population ofcells of the sample;b. delivering reactive primers that are configured to be covalentlyattached to components of the permeabilized cells, thereby creating aplurality of attached primers;c. optionally making genomic DNA of the permeabilized cells or nuclei atleast partially accessible to nucleic acid hybridization;d. delivering cell barcode probes to the permeabilized cells and/ornuclei of the permeabilized cells, wherein a given cell barcode probecomprises a genome binding element shared among the cell barcode probes,and a cell barcode unique for a given cell barcode probe, and whereinthe genome binding element hybridizes to a region in the genomic DNA,thereby forming a nucleic acid duplex between the genome binding elementand the region of the genomic DNA in the cells and/or nuclei;e. removing cell barcode probes that are not bound to the genomic DNAfrom the cells or nuclei, whereby no more than a defined number ofcopies of the cell barcode probe remain in each cell or nucleus;f. amplifying the cell barcodes using the plurality of attached primers,thereby forming amplified cell barcodes within the compartments; andg. attaching the amplified cell barcodes to the macromolecules withincells, thereby forming barcoded macromolecules.

In some embodiments of the disclosed methods, cells or nuclei are fixedwith or before permeabilization. Exemplary methods of fixation areprovided in Examples below.

In preferred embodiments of the disclosed methods, the genome bindingelement is the same for all CBPs delivered to the permeabilized cellsand/or nuclei, so it hybridizes to the same region in the genomic DNA ofthe permeabilized cells and/or nuclei. In these embodiments, thepermeabilized cells and/or nuclei share the same genome binding element.

In preferred embodiments of the disclosed methods, the cell barcode isunique for each CBP that is delivered to the permeabilized cells and/ornuclei, so different CBPs comprise different cell barcodes. When onlyone or two CBPs remain in a cell or nucleus after the removal step,unique cell barcodes of these CBPs are amplified and used to labelcellular macromolecules of a given cell or nucleus, generating barcodedmacromolecules. Unique cell barcodes of CBPs used in each cell ornucleus are preferred to ensure successful tracing of the barcodedmacromolecules back to specific cells or nuclei after analysis of thebarcoded macromolecules.

In a preferred embodiment of the disclosed methods, the CBP barcodes arecomprised of a random nucleotide sequence (via oligonucleotide synthesisusing a mixed base (e.g. N), much like a unique molecular identifier(UMI), but in this case the CBP contains a unique cellular identifier(UCI). In another embodiment, cellular barcode probes (CBPs) arecomprised of UCI barcodes constructed through split-pool synthesis usingchemical synthesis or enzymatic synthesis on beads and subsequentcleavage off of the beads (Delley and Abate. 2021. “Modular BarcodeBeads for Microfluidic Single Cell Genomics.” Scientific Reports 11 (1):10857; Zilionis, et al., 2017. “Single-Cell Barcoding and SequencingUsing Droplet Microfluidics.” Nature Protocols 12 (1): 44-73). In apreferred embodiment, cellular barcode probes (CBPs) constitute alibrary of unique barcodes such that the number of unique barcodes usedin a given cellular labeling experiment exceeds the number of cells byat least tenfold or greater. In this way, “collisions” between cellswith the same barcode are minimized effectively assigning most cells inthe population (an associated analytes therein) to unique barcodes. Inpreferred embodiments, when barcodes are in excess of cells by ten-fold,there is roughly a 5% collision rate; and when in excess of cells byhundred-fold there is less than 0.5% collision rate. This can beexplained by the statistics of the “birthday problem” with the resultingequation (Li and Humphreys. 2021. “Single Cell Technologies: BeyondMicrofluidics.” Kidney360 2 (7): 1196-1204):

${P = {\frac{N - D + {D\left( \frac{D - 1}{D} \right)}^{N}}{N} \sim \frac{N}{2D}{for}{large}N{and}D}},{{{{where}{}P} = {{collision}{rate}}};{N = {{number}{of}{cells}}};{{{and}D} = {{number}{of}{unique}{{barcodes}.}}}}$

For D being tenfold greater than N, P is approximately 5%.

In preferred embodiments of the disclosed methods, the defined number ofunique copies of CBP per cell is one or two copies; thus, after removingcell barcode probes that are not bound to the genomic DNA from thecells, only one or two copies of the cell barcode probe remain in eachcell or nucleus. In some preferred embodiments of the disclosed methods,the defined number of copies is one copy.

As used herein, the defined number of copies is determined beforedelivering cell barcode probes (CBPs) to the permeabilized cells and/ornuclei, based on engineered binding of CBPs or specific genomicDNA-binding carriers comprising CBPs to gDNA of the permeabilized cellsand/or nuclei. In one embodiment, specific genomic DNA-binding carriercarrying CBPs comprising CBPs binds to unique region of the gDNA thatcomprises a polymorphic sequence in one of the chromosomes; thus, only asingle CBP copy will be bound to the gDNA via the carrier and remain inthe permeabilized cells and/or nuclei after removing non-specificallybound or unbound copies (the defined number is one copy). In anotherembodiment, CBPs or specific genomic DNA-binding carriers comprisingCBPs are engineered to bind to unique, non-repetitive region in the gDNAof the permeabilized cells and/or nuclei; in this embodiment, two CBPcopies will be bound to the gDNA (due to duplicate chromosomes) andremain in the permeabilized cells and/or nuclei after removingnon-specifically bound or unbound copies (the defined number is twocopies). In yet another embodiment, CBPs or specific genomic DNA-bindingcarriers comprising CBPs are engineered to bind to a two-copy region inthe gDNA of the permeabilized cells and/or nuclei; in this embodiment,four CBP copies will be bound to the gDNA (due to duplicate chromosomes)and remain in the permeabilized cells and/or nuclei after removingnon-specifically bound or unbound copies (the defined number is fourcopies). Other embodiments include engineered CBPs or specific genomicDNA-binding carriers comprising CBPs that are bound to a repetitiveregion in the gDNA of the permeabilized cells and/or nuclei; in theseembodiments, the defined number is 4, 6, 8, 10, 12, 14, 16, 19, 20, ormore copies.

In the preferred embodiments of the disclosed methods, the sample can beany cellular sample from a biological organism or microorganismincluding tissue, blood cells, cell culture, microbial cells, etc. Insome embodiments, these samples are fixed using any number of standardfixative procedures including formaldehyde-based fixation, Deep EutecticSolvants (DESs), homo-bifunctional crosslinking agents, and others(disclosed in details below).

In preferred embodiments of the disclosed methods, the macromoleculesbeing barcoded can be polypeptides, mRNA molecules or cDNA molecules. Inpreferred embodiments, the macromolecules being barcoded are componentsof cells from the sample, or derivatives of the components of cells fromthe sample (such as cDNA molecules are derivatives of cellular mRNAmolecules).

In some embodiments of the disclosed methods, cell barcode probes aredelivered to the permeabilized cells or nuclei, wherein a given cellbarcode probe comprises a unique cell barcode and a common genomebinding element shared among the permeabilized cells or nuclei, andwherein the genome binding element hybridizes to a region in the genomicDNA, thereby forming a nucleic acid duplex between the genome bindingelement and the genomic DNA in the cells or nuclei. In theseembodiments, interaction between the region in the genomic DNA with thegenome binding element does not induce single-strand breaks ordouble-strand breaks in the genomic DNA. In these embodiments, nocleavage of the genomic DNA is induced or triggered during deliveringcell barcode probes to the permeabilized cells and/or nuclei of thepermeabilized cells and during removing cell barcode probes that are notbound to the genomic DNA from the cells and/or nuclei, since nucleicacid hybridization does not require DNA cleavage. Also, in preferredembodiments, interaction between the region in the genomic DNA with thegenome binding element occurs without exogenous enzymes, such astransposase.

In some embodiments, the disclosed methods further comprise releasingthe barcoded macromolecules from the compartments. In one embodiment,compartments are formed by droplet emulsion, and after attaching theamplified cell barcodes to the macromolecules within the compartments,droplet emulsion is broken releasing the barcoded macromolecules. Insome embodiments, released barcoded macromolecules are collected andused in a high-throughput macromolecule analysis assay, such asProteoCode™ assay.

In some embodiments of the disclosed methods, the region in the genomicDNA used for attachment of CBPs is a non-repetitive region. In preferredembodiments, the non-repetitive region in the genomic DNA is anon-coding region. In other preferred embodiments, the non-repetitiveregion in the genomic DNA is a differentially methylated region that canbe used for targeting of CBPs (more details provided below).

In the disclosed methods, removing cell barcode probes that are notbound to the genomic DNA from the cells and/or nuclei can be performedby various methods known in the art, for example, using posthybridization washing conditions developed for in situ hybridizationmethods. Exemplary non-limiting removal (washing) conditions aredescribed in Examples 5-9. In some embodiments of the disclosed methods,the buffers used in post-hybridization washing and removal of CBPs thatare not bound to the genomic DNA from the cells and/or nuclei are basedon saline-sodium citrate (SSC) buffer (1×SSC buffer comprises 15 mMsodium citrate and 150 mM sodium chloride). The exact concentration ofSSC in the post-hybridization washing solution may need to be optimized.Too much SSC in the washing solution will produce a poor washing effectof low stringency, while too little SSC will tend to wash all CBPs awayfrom the cells and/or nuclei due to high stringency. Temperature and pHalso influence the washing effect; increasing the temperature increasesthe stringency, and the pH determines the availability of the positiveions that counteract the repulsive negative force between the nucleicacid backbones of both the CBP and the genomic DNA. The inclusion of amild non-ionic detergent, such as Tween-20, into the post-hybridizationwashing solution may increase washing efficiency. Some exemplarypost-hybridization washing solutions based on SSC comprise 0.4×SSC at72° C.; 2×SSC with 0.05% Tween at room temperature and solutionsindicated in in Examples 5-9 below. Other (non-SSC-based)post-hybridization washing solutions can also be used that preferablycomprise positively charged ions that counteract the repulsive negativeforce between the nucleic acid backbones of the CBP and the genomic DNA.

In the disclosed methods, partitioning of the cells or nuclei into theplurality of compartments can be performed by various methods known inthe art, for example, disclosed in one of the following patentpublications incorporated herein: US20180355348 A1, U.S. Ser. No.11/441,179 B2, US20190040382 A1, US20210123103 A1, U.S. Ser. No.10/774,370 B2. Methods of partitioning are also disclosed in Examples 13and 14 below.

In the disclosed methods, amplification of the cell barcodes withincompartments can be performed by various methods known in the art. Avariety of known nucleic acid amplification techniques can be used toamplify cell barcodes of CBPs before attaching the amplified cellbarcodes to the macromolecules within the cell. Exemplary non-limitingmethods are described in Examples 14, 15, 17, 19 and 24. Other methodscan be used as well, for example, disclosed in U.S. Ser. No. 10/428,326B2, US20160257984 A1, US20180355348 A1 and U.S. Ser. No. 10/752,895 B2.In some embodiments of the disclosed methods, cell barcodes of CBPs canbe amplified in situ within cells or nuclei (withoutcompartmentalization). Such embodiments will be further discussed below.

In some embodiments of the disclosed methods, the genome binding elementof each cell barcode probe comprises a PCR priming site adjacent to thecell barcode that is used to amplify the cell barcode at step (f).

In some embodiments of the disclosed methods, the sample is a spatialsample (e.g., a tissue slice), and wherein the sample is dissociatedinto a plurality of cells at step (e).

In some embodiments of the disclosed methods, when the sample is aspatial sample, each of the cell barcode probes further comprise apositional barcode different for at least some of the cell barcodeprobes.

In some embodiments of the disclosed methods, the cell barcode probesare delivered at step (c) from a spatially ordered array.

In some embodiments, the disclosed methods further comprise after step(b): (i) delivering a plurality of positional probes to thepermeabilized cells or nuclei, wherein a given positional probecomprises a common targeting element configured to be attached to themacromolecules and a positional barcode different for each positionalprobes; and (ii) attaching positional probes from the plurality ofpositional probes to the macromolecules. In some embodiments, each ofthe amplified cell barcodes comprises a common region that is configuredto hybridize (comprise complementary region(s) configured to formnucleic acid duplexes) to a region in the positional probes; and themethod further comprises a step of performing a primer extensionreaction to transfer the amplified cell barcodes to the positionalprobes attached to the macromolecules. In other embodiments, other waysof attaching amplified cell barcodes to positional probes are used. Insome embodiments, the plurality of positional probes is delivered from aspatially ordered array.

In some embodiments of the disclosed methods, each compartment of theplurality of compartments comprises a compartment barcode configured tobe attached to the macromolecules.

In some embodiments of the disclosed methods, during partitioning thecells or nuclei into the plurality of compartments at step (e), onaverage no more than one cell or nucleus comprising a cell barcode probeis comprised within a single compartment.

In some embodiments of the disclosed methods, attaching the amplifiedcell barcodes to the macromolecules within the compartments comprises:i) covalently attaching nucleic acid recording tags to themacromolecules or macromolecule derivatives of the cell; and (ii)attaching the amplified cell barcodes to the nucleic acid recordingtags.

Barcoding methods presented herein can greatly improve the throughput ofcells and genes detected during single cell RNA or protein sequencing.In some embodiments, cellular barcoding provides for a unique cellularbarcode for all constituent analyte molecules within a single cellacross a population of cells. Sample barcoding (indexing) allows forsample multiplexing, which provides certain advantages for single cellRNA or protein sequencing, such as increased sample throughput in asingle assay, increased number of cells assayed, increased number ofpossible replicates in a single assay. Sample multiplexing refers to thelabeling of a cell or nuclei sample with a sample barcode molecular tagsand subsequently pooling the samples. This set of multiplexed samplescan be processed together. Ideally or preferably, all macromolecules inthe same cell are labeled with the same barcode, while distinct barcodesare used for different cells. After cell processing and macromoleculesequencing, molecular barcode information can be assigned to cells.Overall, barcoding and multiplexing can greatly reduce the processingtime, technical batch effects, and library preparation costs, and lowerthe per-sample cost.

Cellular barcodes can be used to simultaneously tag a number of omicassays including scRNA-Seq assays to measure mRNA abundance, single cellprotein assays such as CITE-Seq, AbSeq, or ProteoCode™ assays(scProt-Seq) to measure protein abundance and modifications, andscATAC-seq or scCut&Tag-seq (see Kaya-Okur, et al., 2019. “CUT&Tag forEfficient Epigenomic Profiling of Small Samples and Single Cells.”Nature Communications 10 (1): 1930) to measure genomic DNA chromatinstate. Various formats of these three Omic assays have been developed.Variations of scRNA-Seq include SMART-Seq, SMART-Seq2, STRT-seq,STRT-Seq-2i, SCRB-seq, mcSCRB-seq, Quartz-seq, Quartz-seq2, Cel-seq,Cel2, MARS-seq, Seq-Well, inDrops, Drop-seq, and other methods. Thesemethods vary primarily in compartment format (plate, nanowell, droplets,etc.) and the single cell barcoding addition step (OligoT primer vs.tagmentation, vs. template switch oligo (TSO) (see Lafzi, Atefeh, etal., 2018. “Tutorial: Guidelines for the Experimental Design ofSingle-Cell RNA Sequencing Studies.” Nature Protocols 13 (12): 2742-57).These difference affect whether full-length transcripts are sequencedand quantified, or just 5′/3′ cDNA tag counting to measure abundance.Likewise, scATAC-seq and scCUT&Tag-seq also has various implementationarchitectures. Exemplary ProteoCode™ assays (scProt-Seq) are describedin US 20190145982 A1.

In some embodiments of the disclosed methods, cell barcodes can be addedat a late stage after macromolecule manipulation in which cells areprocessed individually at early steps (such as reverse transcription,preamplification and tagmentation). Preferably, cell barcodes areattached to macromolecules at an early stage after cell isolation. Then,all cells can be pooled into one single reaction for the following stepsto save cost and labor. The current state-of-art method to labelmacromolecules in a massively parallel scale is to synthesize or loadbarcode molecules on beads such that one single bead carries up to a fewmillion copies of the same barcode molecules, while the barcodesequences on different beads are different (Macosko, E. Z., et al.(2015) Highly Parallel Genome-wide Expression Profiling of IndividualCells Using Nanoliter Droplets. Cell, 161, 1202-1214).

Several DNA-based barcoding methods have been developed for samplemultiplexing during single cell RNA sequencing (reviewed in Cheng J, etat., Multiplexing Methods for Simultaneous Large-Scale TranscriptomicProfiling of Samples at Single-Cell Resolution. Adv Sci (Weinh). 2021September; 8(17):e2101229). The barcodes generated by the describedmethods take advantage of the following processing steps during singlecell RNA sequencing. For example, such barcodes are polyadenylated atthe 3′ end and structurally similar to endogenous mRNA, so they can becaptured by the poly(dT)-containing beads together with other mRNAmolecules in single cell library construction. Alternatively, DNAbarcodes are integrated with mRNA by PCR.

In some embodiments of the disclosed methods, the cellular barcode probeis comprised of a genomic binding sequence (GBS), a forward primersequence, an optional sample hash barcode, a single cell barcode, and areverse primer sequence (see FIG. 7A). The reverse primer sequence mayalso be appended with a “spacer” sequence for use in the ProteoCode NGPAor NGPS assay.

Exemplary flow diagram for barcoding of macromolecules of individualcells showing key steps of the disclosed methods is shown in FIG. 1 .

Another exemplary flow diagram for single cell multi-omics analysisusing nuclei cellular barcode tagging and ePCR is shown in FIG. 2A. Inthese embodiments, the cellular sample is dissociated using proteaseand/or DES treatment and sonication, or other methods known in the art.After collecting the disassociated single cells, the cells arepermeabilized to enable “in situ” access to the cell and nuclearinterior. The steps in grey can be performed in any order and includeprotein tagging with DNA recording tag stubs (rTag), in situ cDNAlabeling, nuclear ATAC-Seq labeling, and nuclear labeling with acellular barcode probe (CBP). FIG. 2B shows a similar workflow for aspatially arrayed biological sample, such as a tissue sample or adherentcells on a slide. An optional spatial encoding step can be implementedwhich attaches a spatial code to the CBP tag or DNA rTags. After spatialencoding, the single cells are dissociated and partitioned intocompartments (e.g., emulsions, droplets, physical compartments, etc.).Emulsion PCR (ePCR) is used to incorporate the CBP tag to the ATAC-Seq,RNA-Seq, and Prot-Seq DNA tags. Finally, amplification primers are usedto prepare scATAC-Seq, scRNA-Seq, and scProt-Seq libraries (for thefollowing NGPA or NGPS assays). Other strategies to incorporate the CBPtag to macromolecules of individual cells can be used and some of themare disclosed below.

In some embodiments of the disclosed methods, the sample is a spatialsample, such as a tissue sample, and cells need to be dissociated fromtissue sample for the following single cell analysis. A number ofmethods can be used to dissociate cells from tissue samples to create apopulation of dissociated cells. Papain treatment is used routinely onfresh tissues to dissociate the sample into discrete cells. A classicprotocol by Huettner and Baughman is described in which tissues areincubated in Papain enzyme solution containing 116 mM NaCl, 5.4 mM KCl,26 mM NaHCO, 1 mM NaHPO, 1.5 mM CaCl2), 1 mM MgSO2, 0.5 mM ETDA, 25 mMglucose, 1 mM systeine, and 200 U papain (Cooper Biomedical, MalvernPa.) for 1 hr at 37° C. (Huettner, J. E., and R. W. Baughman. 1986.“Primary Culture of Identified Neurons from the Visual Cortex ofPostnatal Rats.” The Journal of Neuroscience: The Official Journal ofthe Society for Neuroscience 6 (10): 3044-60). This reagent is providedin commercial form as the Worthington Papain Dissociation System(Worthington Biochemical Corporation). Other proteases of utility inassisting with tissue dissociation include: Liberases (Roche),Collagenase Type I, II, III, or IV, Trypsin, Proteinase K, Chymotrypsin,Elastase, Dispase, Pronase (Sigma).

In other embodiments of the disclosed methods, methods to simultaneouslyfix and dissociate cells can be employed. Rapid fixation maintains RNAand protein integrity. The ACME dissociation protocol is comprised oftreating cells with a solution of acetic acid, methanol, and glycerol inwater. Moreover, ACME-treated cells can be easily cryopreserved in DMSO(10%) for later single cell processing. Additionally, ACME can be usedto fix trypsin or papain dissociated cells as described above.

In some embodiments of the disclosed methods, tissue fixation can beachieved using Deep Eutectic Solvents (DESs) (U.S. Pat. No. 9,696,247B2, included by reference), which can also can aid in tissuedissociation. DESs have the ability to uniquely fix cells and stabilizetheir molecular components such as RNA, DNA, proteins, carbohydrates,and metabolites. A commercial example of a DES-based fixation reagent isvivoPHIX (RNAssist, UK). In one embodiment, the first component is aquaternary ammonium or phosphonium compound such as choline chloride orN, N, N-trimethylglycine (betaine), and wherein the second component isa hydrogen bond donor, such as urea, trifluoroacetamide, ortrifluoropropanamide. In a preferred embodiment, a deep eutectic solventis comprised of choline chloride: 3,3,3-trifluoroacetamide, optionallyin a molar ratio of about 1:2; choline chloride:2,2-difluoro-2-phenylacetamide, optionally in a molar ratio of about1:1; choline chloride:trehalose, optionally in a molar ratio of about1:1 and butyrylcholine iodide: urea, optionally in a molar ratio ofabout 1:2. In another embodiment, the addition of 1-33 mM, preferably−10 mM of Zinc salts such as Zinc chloride, Zinc sulphate or Zinccitrate to the Choline chloride: Trifluoroacetamide improves cellfixation rates. In a preferred embodiment, the DES reagent also containsa detergent additive to aid in cell membrane permeabilization. Exemplardetergent additives include digitonin, saponin, TX-100, NP-40, andTween-20. In another embodiment, the cells can be first cross-linkedusing exposure to a 1-6% paraformaldehyde solution for 10 min-1 hr atroom temperature. Alternatively, the crosslinking can also be performedafter DES treatment. In addition to fixing cells, DES solvents alsoweaken interactions between cells to facilitate dissociation of tissuesinto single cells in solution. In a preferred embodiment, cells ortissues are placed in a DES solvent and dissociated by sonication. In apreferred embodiment, tissues or cells that have been fixed withtrimethylglycine:trifluoroacetamide (1:2) are dissociated into singlecells under mild sonication preserving the integrity of macromoleculestherein.

There are a variety of described methods to label a single copy locuswithin the genome using in situ hybridization (ISH) or fluorescence insitu hybridization (FISH) approaches (for example, disclosed in U.S.Pat. Nos. 5,447,841, 5,948,617; De Bau, L. E., and J. Gu. 1996. “IN SITUHYBRIDIZATION, IN SITU TRANSCRIPTION, AND IN SITU POLYMERASE CHAINREACTION.” Scanning Microscopy 10 (Article 3): 27-47; Beliveau, B. J.,et al. 2015. “Single-Molecule Super-Resolution Imaging of Chromosomesand in Situ Haplotype Visualization Using Oligopaint FISH Probes.”Nature Communications 6 (May): 7147). These methods typically employeenucleic acid probes which hybridize to a defined target region orregions within the genome. In some embodiments, hybridization ofcellular barcode probes (CBPs) to target genomic sequences can beaccomplished using standard ISH/FISH techniques. The key steps inISH/FISH are generally as follows: 1) fixation and permeabilization ofthe cells or tissue (in solution or on a slide) to be analyzed; 2)pre-hybridization treatment of fixed/permeabilized cells or tissue todenature genomic DNA (gDNA) or render regions of the gDNA singlestranded; 3) blocking of cells or tissue to minimize non-specificbinding of FISH probes; 4) hybridization of FISH probes to the gDNAwithin the permeabilized cells/tissue; and 5) post-hybridization washesto remove non-specifically bound FISH probes. In some embodiments ofdescribed barcoding methods, the cell barcode of the CBP will beamplified and used to label constituent molecules within the cell forsingle cell applications.

Nucleic acid ISH/FISH probes are typically comprised of DNA, LNA, PNA,or RNA, and are designed to be complementary to the genomic sequence ofinterest. LNA-FISH and PNA-FISH can be used to generate probesexhibiting higher binding affinity, greater strand invasion properties,and shorter hybridization times than standard DNA probes with aresulting more intense FISH signal (Genet, M. D., et al., 2013. “DirectDNA and PNA Probe Binding to Telomeric Regions without Classical in SituHybridization.” Molecular Cytogenetics 6 (1): 42).

A key challenge in ISH/FISH protocols is to efficiently hybridize theprobe to intrinsically double stranded genomic DNA. A standard method toenable efficient hybridization genomic DNA is to denature the DNA togenerate a ssDNA annealing site for the ISH/FISH probe (Shakoori, 2017,“Fluorescence In Situ Hybridization (FISH) and Its Applications.” InChromosome Structure and Aberrations, edited by Tariq Ahmad Bhat andAijaz Ahmad Wani, 343-67. New Delhi: Springer India). This denaturationis typically accomplished using heat and chemical denaturants such aformamide or urea, or via the use of polar aprotic solvents such asethylene carbonate (disclosed in U.S. Pat. No. 9,303,287 B2, U.S. Pat.No. 9,388,456 B2, U.S. Pat. No. 9,309,562 B2, U.S. Ser. No. 10/202,638B2 all incorporated by reference). In one example, ethylene carbonate, apolar aprotic solvent, acts as an effective replacement for formamide inDNA hybridization buffers and improves both the rate of hybridizationand reduces the background when included in hybridization and/or washbuffers (U.S. Pat. No. 9,309,562 B2, U.S. Ser. No. 10/202,638 B2,incorporated herein by reference).

In some embodiments of the disclosed methods, there is no need toseparately denature the genomic DNA but rather the use of appropriatedenaturing buffers (e.g., comprised of ethylene carbonate) or strandinvading probes (e.g., PNA, recA-coated DNA) enables labeling of genomicDNA without using a specific denaturation step.

A large number of methods for more efficient labeling of genomic DNAwithin fixed/permeabilized cells or tissues have also been described(Genet, M. D., et al., 2013. “Direct DNA and PNA Probe Binding toTelomeric Regions without Classical in Situ Hybridization.” MolecularCytogenetics 6 (1): 42; Clyde, Dorothy. 2021. “Targeted Local DNADenaturation with GOLD FISH.” Nature Reviews. Genetics 22 (5): 267-267;Wang, et al., 2021, “Genome Oligopaint via Local DenaturationFluorescence in Situ Hybridization.” Molecular Cell 81 (7):1566-1577.e8). These include physicochemical and enzymatic methods forcreating localized regions of ssDNA at the locus of interest.Physicochemical methods include the use of strand invasion/displacementand D-loop formation tools such as using RecA coated probes, Bis-PNAstrand openers, triple helix formation probes, and padlock probes tostabilize the invading probe structure (Matsunaga and Matsunaga, 2017,“FISH with Padlock Probes Can Efficiently Reveal the Genomic Position ofLow or Single-Copy DNA Sequences.” Cytologia 82 (4): 337-39; Yaroslavskyand Smolina, 2013, “Fluorescence Imaging of Single-Copy DNA Sequenceswithin the Human Genome Using PNA-Directed Padlock Probe Assembly.”Chemistry & Biology 20 (3): 445-53; Gruenig, et al., 2011, “CreatingDirected Double-Strand Breaks with the Ref Protein: A NovelRecA-dependent Nuclease From Bacteriophage P1” The Journal of BiologicalChemistry 286 (10): 8240-51). Improved bioinformatic probe design andalternative probe FISH probe architectures such as padlock probes havealso improved signals from FISH assays (Yaroslavsky and Smolina, 2013,“Fluorescence Imaging of Single-Copy DNA Sequences within the HumanGenome Using PNA-Directed Padlock Probe Assembly.” Chemistry & Biology20 (3): 445-53).

In some embodiments of the disclosed methods, CBPs are linearpolynucleotides. In other embodiments, a padlock CBP can be employed. Apadlock probe is a linear polynucleotide comprising complementarysequence arms to the target region; ligation (and optional extension) ofthe left and right arms upon target annealing generates a circularizedpadlock probe. Padlock probes combined with rolling-circle amplificationenable fluorescence in situ hybridization (FISH) to reproducibly detectthe genomic position of low or single-copy DNA sequences (Matsunaga andMatsunaga, 2017). The use of a padlock probe improves specificity duringin situ hybridization by requiring ligation of the two arms of thepadlock probe to create a circular construct.

In preferred embodiments of the disclosed methods, after delivering CBPsto the permeabilized cells and/or nuclei, and attaching the CBP to gDNAby forming a nucleic acid duplex or binding to a region in gDNA, excessof CBPs that includes unbound or nonspecifically bound CBPs are removedby washing. Some specific conditions for washing out excess of CBPs aredisclosed in Examples 5, 8 and 12. In some preferred embodiments, thewashing conditions post-CBP hybridization or binding to the gDNA, employhigh-stringency washing conditions to removed mis-hybridized ornon-specifically bound CBP complexes. Typical stringency parametersoptimized in a wash optimization include the following: 1) saltconcentration and type; 2) addition of denaturants such as formamide,ethylene carbonate, urea, DMSO, etc.; 3) temperature; and 4) presenceand type of detergents employed. The choice of hybridization and washstringency conditions will be inextricably linked to the probe design.In general, optimal hybridization stringency generally occurs at atemperature 10-25° C. lower than the probe melting temperature (Tm) inthe hybridization buffer employed. Nucleic acid probe meltingtemperature is determined intrinsically by the nucleic acid compositionand length of the probe, and extrinsically by the buffer composition andtemperature.

Enzymatic methods of creating ssDNA regions include the use ofrestriction enzyme digestion (or CRISPER-Cas systems for targetedendonuclease digestion) combined with ExoIII to create ssDNA regions forhybridization, or restriction enzyme digestion combined withrecA-mediated strand invasion at the ends of gDNA (Matsunaga andMatsunaga, 2017). CRISPER-Cas systems can also be used to targetendonuclease cleavage at defined sites in the genome such as the abilityto generate site-specific localized denaturation using aCas9-topoisomerse fusion protein described in GOLD-FISH technique byWang et al. (Wang, et al., 2021. “Genome Oligopaint via LocalDenaturation Fluorescence in Situ Hybridization.” Molecular Cell 81 (7):1566-1577.e8).

The efficiency of probe annealing to gDNA during in situ hybridizationis greatly enhanced by linearizing the gDNA in the region to which theprobe anneals. A number of different methods have been employed togenerate a ssDNA site for probe annealing. One method is to employ anexonuclease-based approach using site-specific restriction endonucleasesto generate free dsDNA termini suitable as a substrate for exonucleaseIII (ExoIII) digestion of the 3′ strand (Matsunaga and Matsunaga, 2017).These ExoIII-linearized regions can also be used as targets for bothhybridization and ligation of CBPs appropriately designed. Namely, afterendonuclease digestion, a given gDNA site can be targeted with apartially double stranded CBP having a 5′ overhang such that CBP isligated onto the nascent cleaved ss-gDNA sequence or is stablyhybridized to the sequence (see FIG. 5 ). Alternative to exonuclease IIIdigestion, the CBP can be coated with RecA to enable strand invasion ofthe 3′ gDNA fragment at the blunt end of the digestion site.

Another method to locally expose a single strand region in the gDNA isto incubate the gDNA within the cells with Bis-PNA openers which willbind to the antisense strand to the probe and create an ssDNA region forlinear or padlock probe annealing (Gyllborg, Daniel, et al., 2020,“Hybridization-Based In Situ Sequencing (HybISS): Spatial TranscriptomicDetection in Human and Mouse Brain Tissue.” Nucleic Acids Research,Volume 48, Issue 19, Page e112).

More recently, methods of labeling genomic loci without the need toseparately create ssDNA have also been described with the most prominentmethods employing CRISPR-Cas based approaches using catalyticallyinactive Cas nucleases for locus-specific labeling, such as CASFISH,CAS-liveFISH, and CRISPR/Cas9-based RGEN-ISL. These approaches employ acatalytically inactive Cas nucleases (dCas) which serve as a gRNA-guidedtargeted binding proteins (see, for example, US 20190330678 A1, U.S.Ser. No. 10/767,168 B2, U.S. Ser. No. 11/124,782 B2, U.S. Ser. No.10/858,639 B2 all incorporated by reference). The binding of thedCas-gRNA protein complex to the gDNA is quite stable (slow off-ratewith dissociation half-life of more than 2 days), making it a suitableprobe for in situ labeling approaches (Boyle, et al., 2017.“High-Throughput Biochemical Profiling Reveals Sequence Determinants ofdCas9 off-Target Binding and Unbinding.” Proceedings of the NationalAcademy of Sciences of the United States of America 114 (21): 5461-66).In one example, inactive dCas9 nuclease is comprised of D10A and H840Aendonuclease inactivating mutations relative to the Streptococcuspyogenes wildtype Cas 9 sequence; dCas9 (and various homologs) areavailable from several commercial sources such as Novateinbio, AppliedBiological Materials (ABM), IDT, and New England Biolabs (NEB). ThedCas9 variants are also commercially available with various N-terminalfusions to enable easy labeling with fluorophores or DNA tags includinga dCas9 SNAP-tag version from NEB.

In some embodiments of the disclosed methods, other fusion proteins canalso be attached to dCas9 such as a dCas9-SpyCatcher fusion that can beused to enable covalent labeling with a CBP-SpyTag conjugate. In someembodiments, CBP is directly attached to inactive dCas9 nuclease; inother embodiments, the gRNA can be labeled with CBP either by directinclusion (e.g. gRNA comprises, or consists of CBP) or indirectly viahybridization. When the CBP is incorporated into the gRNA, the CBP canbe annealed to a hybridization region on the gRNA or the gRNA can becomprised of the CBP RNA sequence. An exemplary resource for design ofgRNAs for CRISPR targeting applications, including using dCas nucleasesas specific gDNA-binding proteins, is the CHOPCHOP webtool and database(Labun, et al., 2021, “CRISPR Genome Editing Made Easy Through theCHOPCHOP Website.” Current Protocols 1 (4): e46).

In some embodiments of the disclosed methods, a number of othercatalytically inactive Cas9 variants and homologs can be employed forsequence-specific binding to gDNA, including more recently developedhigher fidelity Cas9 variants with greatly reduced off-target activityincluding SpCas9-HF1(N497A, R661A, Q695A, Q926A) or eSpCas9-1.1 (N497A,R661A, Q695A, K848A, Q926A, K1003A, and R1060A) (Slaymaker, et al.,2016. “Rationally Engineered Cas9 Nucleases with Improved Specificity.”Science 351 (6268): 84-88) and HypaCas9 (N692A/M694A/Q695A/H698A)(Kleinstiver, et al., 2016. “High-Fidelity CRISPR-Cas9 Nucleases with NoDetectable Genome-Wide off-Target Effects.” Nature 529 (7587): 490-95).Additionally, Cas9 variants with a relaxed PAM sequence requirement suchas XCas9 variants may also be useful (Hu, et al., 2018. “Evolved Cas9Variants with Broad PAM Compatibility and High DNA Specificity.” Nature556 (7699): 57-63). These gene variants are available from Addgene(Watertown, Mass.) and can be rendered catalytically inactive by portingD10A and H840A mutations or equivalent mutations (depending onhomologue) to the respective Cas sequence. Cas9 nickases containingeither D10A (coding strand) or H840A (non-coding strand) can also beemployed for facilitating strand invasion.

In some embodiments of the disclosed methods, Cas9 homologues fromdifferent organisms can also be employed, including Streptococcuspyogenes (Sp), Staphylococcus aureus (Sa), Neisseria meningitidis (Nm orNme), Campylobacter jejuni (Cj), Streptococcus thermophilus (St),Treponema denticola (Td). These Cas9 homologues differ in their PAMsequence and gRNA requirement which needs to be considered in selectionof the targeted sequence in gDNA. In other embodiments, the greaterCRISPR-Cas nuclease systems (and inactive enzyme variants) can also beused for site-specific genomic DNA cleavage (or labeling viacatalytically inactive engineered Cas nuclease). The CRISPR-Casendonucleases systems are found among different species of bacteria,bacteriophages, and archaea and include Cas9, Cas12a, Cas12b, Cas14,CasX, CasPhi and others. Most of the Cas enzymes used for gene editingare classified as TypeII and are characterized by a single large Casdomain responsible for sgRNA binding and targeted endonuclease activity.

In other embodiments of the disclosed methods, in addition tocatalytically inactive RNA-guided Cas9 proteins, other specific genomicDNA-binding carriers can be employed. Many different enzymes thatrecognize specific genomic DNA regions are known in the art and can beutilized in the disclosed methods to deliver CBPs to the permeabilizedcells or cell nuclei. Some non-limiting examples of genome editingenzymes, such zinc finger nucleases, meganucleases and Transcriptionactivator-like effector (TALE) nucleases (TALENs), are disclosed, inU.S. Pat. Nos. 9,695,432, 9,499,592, 9,393,257, 9,315,788, 9,187,758,8,921,112, 8,906,607, 8,771,945, 8,697,853, 8,163,514, 8,119,381,8,420,782, 8,440,432, 8,440,431, 7,888,121, 7,241,573, which can beappropriately modified and adopted for the barcoding methods disclosedherein.

In some embodiments of the disclosed methods, a nuclease-deficientArgonaute protein can be attached to a CBP to target specific genomicloci of individual cells as described by Chang et al in a techniquecalled agoFISH (Chang, Lei, et al., 2019. “AgoFISH: Cost-Effective inSitu Labelling of Genomic Loci Based on DNA-Guided dTtAgo Protein.”Nanoscale Horizons 4 (4): 918-23). In one embodiment, a guide DNAcomprises a 5′ phosphate and a CBP sequence that comprises a barcode anda target for dTtAgo protein. dTtAgo protein can specifically target(without cleavage) genomic DNA sequences using a ssDNA guide DNA of˜16-24 nt in length with a 5′ phosphate moiety (Chang, Lei, et al.,2019). Attachment of CBP to dTtAgo can accelerate target findingcompared to a naked CBP nucleic acid. Mutations in the catalyticaspartate residues of the Ago protein render it nuclease deficient, yetcapable of target-specific binding of DNA in the presence of a guideDNA/RNA. Exemplar engineered nuclease-deficient prokaryotic Argonauteproteins (pAgos) include engineered pAgos from thermophilic bacteriaThermus thermophilus, Pyrococcus furiosus, Methanocaldococcusjannaschiil; and mesophilic bacteria Clostridium butyricum, Limnothrixrosea, Synechococcus elongatus, and Kurthia massiliensis (Kropocheva,Ekaterina, et al., 2021. “A Programmable pAgo Nuclease with UniversalGuide and Target Specificity from the Mesophilic Bacterium KurthiaMassiliensis.” Nucleic Acids Research 49 (7): 4054-65).

In some embodiments of the disclosed methods, Prime Editing (PE) can beadapted for inserting CBPs into a gDNA. In PE, a “nicking” Cas9 (H840A)fused to a reverse transcriptase employs a 3′-extended guide RNA, termedpegRNA, which enables targeted insertion of a region at the 3′ end ofthe pegRNA copied onto the non-complementary nicked strand via its 3′flap acting as a primer for RT extension (Anzalone, et al., 2019,“Search-and-Replace Genome Editing without Double-Strand Breaks or DonorDNA.” Nature 576 (7785): 149-57).

In some embodiments of the disclosed methods, after delivery of a CBP topermeabilized cells, the genome binding element of the CBP hybridizes toa non-repetitive region in the genomic DNA (gDNA) of the cells, therebyforming hybridization duplexes between the genome binding element andthe gDNA in the cells.

In some embodiments of the disclosed methods, hybridization between thegenome binding element of the CBP and gDNA within fixed/permeabilizedcells is achieved using chemical denaturation or an enzymatic process torender target regions of gDNA at least partially accessible to nucleicacid hybridization. Partially accessibility to nucleic acidhybridization refers to a partial unfolding of double stranded gDNA,which exposes one of the strands to interaction with a portion of CBPand eventually to formation of nucleic acid duplex between the portionof CBP and one of the strands of gDNA. Exemplary methods to producepartially accessibility to nucleic acid hybridization are disclosed inExamples below, and other methods can also be used. gDNA of thepermeabilized cells or nuclei can be made partially accessible tonucleic acid hybridization in a separate step of the disclosed barcodingmethods, or it can be made during hybridization with CBPs. In preferredembodiments, partially accessibility to nucleic acid hybridization canbe achieved by utilizing reaction conditions designed for nucleic acidhybridization, such as conditions described in Example 5.

In some embodiments of the disclosed methods, the CBPs are designed tohybridize to non-transcribed regions of the genome to preventinteraction with transcribed mRNA in the cell.

In some embodiments of the disclosed methods, hybridization of CBPs canbe accomplished by in situ hybridization methods as described in U.S.Pat. Nos. 5,447,841 A and 5,948,617 A. Namely, the major steps involvedin in situ hybridization are as follows: 1) cell fixation andpermeabilization; 2) pre-hybridization treatment to at least partiallydenature gDNA and increase gDNA accessibility; 3) optional blocking stepto reduce background; 4) hybridization of probe to gDNA within cells; 5)and post-hybridization washes to remove non-specifically bound probes.After in situ hybridization of the CBPs, the cells can be disassociated(e.g., tissue section on slide) and employed in single cell barcodingmethods described below.

In some embodiments of the disclosed methods, the genome binding elementof CBP comprises modified nucleotides or nucleotide analogs capable ofhybridizing (forming multiple hydrogen bonds) with genomic DNA. In someembodiments, the genome binding element comprises a PNA (peptide nucleicacid) molecule (see e.g., Example 7 below). The advantage of using PNAsis reducing size of the genome binding element. In some embodiments, thegenome binding element of CBP comprises between 5 and 100 nucleotides ornucleotide analogs. In some embodiments, the genome binding element ofCBP comprises between 10 and 100, between 10 and 70, between 10 and 50,between 10 and 40, between 10 and 30, between 20 and 70, or between 20and 50 nucleotides or nucleotide analogs.

In some embodiments of the disclosed methods, cell fixation isaccomplished with exposure to formaldehyde/para-formaldehyde whichcross-links cellular proteins and anchors soluble proteins to thecytoskeleton to preserve cell structure. Additionally, formaldehydefixation maintains cell morphology and enables generation of robust ISHsignals. In some embodiments, permeabilization of intact cells can beachieved when formaldehyde is used in combination with a membranesolubilizing reagent such as nonionic detergents (e.g., Tween20) andalcohols (e.g., methanol). Alcohols fix cells by proteinprecipitation/denaturation and can be enhanced when used in combinationwith acetic acid (Carnoy's fixative or ACME fixative).

In some embodiments of the disclosed methods, ISH probe binding to ahaploid imprinted loci or X-chromosome inactivated loci using MeFISH canbe utilized for delivering a single copy of CBPs to gDNA of thepermeabilized cells. In mammals, a small subset of genes and intergenicregions are differentially methylated between parental alleles leadingto parent-of-origin-specific gene expression. Imprinted loci on thegenome are comprised of symmetric CpG methylation of both strands of oneparental allele and non-methylation at the other parental allele (Tucci,et al., and Erice Imprinting Group, 2019, “Genomic Imprinting andPhysiological Processes in Mammals,” Cell, 176 (5): 952-65). Using thefact that only one of the two parental alleles is imprinted ormethylated, one can use MeFISH-like approaches to specifically hybridizeand cross-link a CBP to the methylated locus enabling tagging of thegenome with only a single copy of the CBP per cell.

MeFISH works by employing DNA probes designed with an adenine baselabeled with a bipyridyl chelator moiety directly facing the cytosinebase being queried with regard to its methylation status (see FIG. 10 ).An adenine base labeled with a bipyridyl moiety chelates osmiumtetroxide and covalently attaches to opposing methyl cytosine bases (seeBuchmuller, et al., 2021. “Programmable Tools for Targeted Analysis ofEpigenetic DNA Modifications.” Current Opinion in Chemical Biology 63(August): 1-10). After probe hybridization, the cells are incubated withosmium tetroxide, which is chelated by the bipyridyl group on the probeand will form a covalent adduct with methyl cytosine, but not withunmethylated cytosine, effectively cross-linking the probe in place.Uncross-linked probe is washed away. In some embodiments, CBPs can bedesigned to label on a single locus with one copy of the CBP probe percell.

Exemplar imprinted genes and genomic regions in humans which can be usedas CBP probe targets for single copy genomic labeling are shown below(based on Tucci, et al., 2019, Cell, 176 (5): 952-65): DIRAS3, IL12RB2,RNU5D-1, AGO1, UTS2, THAP3, CACNA1E, CYP2J2, ACOT11, LINC00467, LRRTM1,TMEM247, THUMPD2, PAX8, PAX8-AS1, DNAH7, ICA1L, GPR1, GPR1-AS, ZDBF2,MRPL44, SPHKAP, USP4, SLC4A7, ZNF385D, EFCC1, RAB7A, MCCC1, FGF12, MFI2,GPR78, STX18-AS1, PDE6B, SH3BP2, NAP1L5, GRID2, SFRP2, FAM149A, FRG1,PLEKGH4B, RHOBTB3, NUDT12, VTRNA2-1, ZNF354C, CUL7, MDGA1, MOCS1,C6orf47, RNF144B, CD83, FAM50B, FAM50B-AS, AIM1, LIN28B, PHACTR2, HYMA1,PLAGL1, SLC22A2, SLC22A3, PLG, KIF25, GRB10, RAPGEF5, SCIN, THSD7A,CALCR, TFPI2, SGCE, PEG10, PDK4, CPA4, MEST, MESTITI, COPG2IT1, KLF14,KLHDC10, AGBL3, PRKAG2, PTK2B, R3HCC1, CLDN23, DLGAP2, PKIA, ZFAT,ZFAT-AS1, PEG13, PSCA, NAPRT1, TRAPPC9, KCNK9, DENND3, GLIS3,PGM5P3-AS1, EXD3, PTCHD3, ITGA8, PROSER2, PROSER2-AS1, JMJD1C, AIFM2,USMG5, VWA2, INPP5F_V2, CPXM2, ACCS, ALKBH3, MAPK8IP1, WT1-Alttranscript, WT1AS, LINC00294, miR-675, IGF2, IGF2AS, INS, KCNQ1,KCNQ10T1, KCNQ1DN, CDKN1C, PHLDA2, miR-483, SLC22A18, ZNF215, NAV2,ART5, OVCH2, RNF141, IRF7, ANO1, PAK1, VSTM5, ZC3H12C, SPA17, NTM,OPCML, TIGAR, CACNA1C, WIF1, N4BP2L1, RB1, RB2, LPAR6, DLEU7, KLHL1,FGF14, PCK2, PAPLN-AS1, DLK1, MEG3, MIR337, RTL1, MEG8, miR-134, PiRNAs,MKRN3, MAGEL2, NDN, NPAP1, SNURF, SNRPN, SNORD107, SNORD64, SNORD108,SNORD109A, SNORD116@, IPW, SNORD115@, SNORD109B, UBE3A-AS, UBE3A, PWRN1,SNHG14, H73492, RYR3, DNM1P35, RASGRF1, FAM174B, IRAIN, LRRK1, SIAH1,ZNF597, NAA60 isoform 1, PDPR, ZFP90, CLEC3A, NLGN2, SEPT4, ZNF714, AXL,DNMT1, SIPR2, ICAM1, FDX1L, ZNF833P, GNG7, ANO8, CACNA1A, C19MC, ZNF331,Anti-MIR371-MIR373, MIR512-1, ZIM2, PEG3, MIMT1, ZNF542P, CST1,PSIMCT-1, ACTL10, NNAT, BLCAP, ZHX3, L3MBTL, SGK2, CYP24A1, NESP55,GNASXL, Epxon-1A, GS-alpha, SANG, miR-296, miR-298, GDAP1L1, PRMT2,CBR1, TPTEP1, ARVCF, CACNA11, NHP2L1, SLC9A7.

In some embodiments of the disclosed methods, CBP probe binding usingISH protocols (via nucleic acids, DNA binding proteins, etc.) to analtered cancer-specific genomic lesion (variant or epigeneticmodification) within the permeabilized cells enables targeted analysisof cancerous cells such as CTCs or other tumorous cells. Only cells withthe genomic alterations will be labeled with CBPs and subsequentlygenerate NGS multi-omic libraries for analysis. These cancer-specificprobes can be designed to specific genetic lesions such as mutationalvariants, or in a preferred embodiment, be designed to bind in amethylation-dependent manner. Tumor suppressor genes such as p53,BRCA1/BRCA2, APC, PTEN, etc. are known to undergo hypermethylation, somein an allele-specific manner, during tumorigeneses forming a suitabletarget by CBP labeling.

In yet another embodiment, provided herein is a method for barcodingmacromolecules from a sample comprising a population of cells, themethod comprising the following steps:

a. permeabilizing cells, or nuclei of the cells, from the population ofcells of the sample;b. delivering a specific genomic DNA-binding carrier comprising a cellbarcode probe to the permeabilized cells or nuclei, wherein a given cellbarcode probe comprises a cell barcode unique for each cell or nucleus,and a priming site, and wherein the specific genomic DNA-binding carrierspecifically binds to a region in the genomic DNA of the cells ornuclei;c. removing specific genomic DNA-binding carriers that are not bound tothe genomic DNA from the cells or nuclei, whereby no more than a definednumber of copies of the cell barcode probe remain in each cell ornucleus;d. amplifying the cell barcodes that were not removed from the cells ornuclei at step (c), thereby forming amplified cell barcodes; ande. attaching the amplified cell barcodes to the macromolecules, therebyforming barcoded macromolecules.

In some embodiments of the disclosed methods, the specific genomicDNA-binding carrier comprises a catalytically inactive Cas nuclease, aTALE protein or a zinc-finger protein.

In some embodiments of the disclosed methods, amplifying the cellbarcodes at step (d) comprises providing conditions for hybridizationbetween the cell barcode probes and a plurality of attached primers.

In preferred embodiments of the disclosed methods, the defined number ofcopies of CBP is one copy or two copies; thus, after removing specificgenomic DNA-binding carriers that are not bound (or nonspecificallybound) to the genomic DNA from the cells, only one copy or two copies ofthe cell barcode probe remain in each cell.

In the disclosed methods, the macromolecules being barcoded can bepolypeptides, mRNA molecules or cDNA molecules. In preferredembodiments, the macromolecules being barcoded are components of cellsfrom the sample, or derivatives of the components of cells from thesample (such as cDNA molecules are derivatives of cellular mRNAmolecules).

In some embodiments of the disclosed methods, the region in the genomicDNA used for attachment of CBPs is a non-repetitive region. In preferredembodiments, the non-repetitive region in the genomic DNA is anon-coding region. In other preferred embodiments, the non-repetitiveregion in the genomic DNA is a differentially methylated region that canbe used for targeting of CBPs (more details provided below).

In some embodiments, each of the cell barcode probes further comprises apositional barcode different for at least some of the cell barcodeprobes.

In some embodiments, the specific genomic DNA-binding carrier(s) is/aredelivered at step (b) from a spatially ordered array.

In some embodiments of the disclosed methods, step (d) further comprisesthe following steps: (i) partitioning the cells or nuclei into aplurality of compartments; and (ii) amplifying the cell barcodes withincompartments of the plurality of compartments, thereby forming amplifiedcell barcodes within the compartments.

In some embodiments, during partitioning the cells or nuclei into theplurality of compartments, on average no more than one cell or nucleuscomprising a cell barcode probe is comprised within a singlecompartment.

In some embodiments, at step (d) the cell barcodes are amplified in situwithin cells or nuclei, and without partitioning the cells or nucleiinto the plurality of compartments.

In some embodiments, the cell barcode probe is integrated in the genomicDNA of the cells or nuclei at step (b).

In some embodiments, the genome binding element of each cell barcodeprobe comprises a PCR priming site adjacent to the cell barcode that isused to amplify the cell barcode at step (d).

In some embodiments, the sample is a spatial sample (e.g., a tissueslice).

In some embodiments, each of the cell barcode probes further comprise apositional barcode different for at least some of the cell barcodeprobes.

In some embodiments, each compartment of the plurality of compartmentscomprises a compartment barcode configured to be attached to themacromolecules.

In some embodiments, attaching the amplified cell barcodes to themacromolecules within the compartments comprises: i) covalentlyattaching nucleic acid recording tags to the macromolecules ormacromolecule derivatives of the cell; and (ii) attaching the amplifiedcell barcodes to the nucleic acid recording tags.

In some embodiments, programmable DNA binding proteins such as designedTALE (dTALE) or zinc-finger proteins can be used to bind a specific DNAlocus within the genome. dTALE proteins are characterized by tandem34-amino acid repeats which recognize one base pair each and directsequence-specific DNA binding through designed concatenation of repeatvariable di-residues (RVDs). The particular order and composition of theRVDs comprise a TALE DNA binding code' in which robust comprehensiverules of DNA recognition are known; A NI binds A, HD binds C, NN/NKbinds G, and NG binds T. As such, sequence-specific DNA binding can beachieved by simple assembly of these 4 or 5 individual RVD repeats withdesired base specificities. dTALE proteins comprised of NG, HD and NNRVDs bound their targets with high affinity (160 pM-2.4 nM) (Meckler, etal. 2013. “Quantitative Analysis of TALE-DNA Interactions SuggestsPolarity Effects.” Nucleic Acids Research 41 (7): 4118-28). dTALES canalso be designed to be methylation specific enabling binding to anon-methylated allele and not to a methylated allele allowing haploidgenome labeling (Tsuji, et al., 2018. “Sequence-Specific 5mC Detectionin Live Cells Based on the TALE-Split Luciferase ComplementationSystem.” The Analyst 143 (16): 3793-97). Crosslinking of the dTALEproteins to the bound DNA will stabilize the complex. This can beaccomplished using a psoralen cross-linker attached to the dTALEprotein. Psoralen intercalates AT dinucleotides and crosslinksjuxtaposed Ts' in an AT dinucleotide duplex (Bornet, et al., 1995.“Solution Structure of Oligonucleotides Covalently Linked to a PsoralenDerivative.” Nucleic Acids Research 23 (5): 788-95). Exemplary methodsfor preparing Transcription activator-like effector (tale) libraries anddetermining a TALE that binds to a given nucleotide sequence aredisclosed in US20160369268 A1 (incorporated herein).

In some embodiments, there is no partitioning of the cells or nucleifrom the cells into a plurality of compartments before amplification ofthe cell barcodes. In these embodiments, CBPs can be amplified by insitu PCR (as described in Bagasra, Omar. 2007. “Protocols for the inSitu PCR-Amplification and Detection of mRNA and DNA Sequences.” NatureProtocols 2 (11): 2782-95; Athman, et al., 2014. “Protocol: A Fast andSimple in Situ PCR Method for Localising Gene Expression in PlantTissue.” Plant Methods 10 (September): 29) or bridge amplification (see,for example, U.S. Pat. No. 7,115,400 B1). For example, for tissuesection sample, the CBP hybridized to gDNA is amplified and subsequentlyattached to the constituent macromolecules containing a DNA recordingtag using in situ PCR techniques as described in Bagasra, 2007,“Protocols for the in Situ PCR-Amplification and Detection of MRNA andDNA Sequences”, Nature Protocols 2 (11): 2782-95. Namely, the recordingtags (CBP_(F)) are attached to macromolecules (e.g. proteins) usingstandard bioconjugation techniques as described in Example 20. The rTagCBP_(F) primer attached to the macromolecule acts a primer in the insitu PCR reaction comprised of solution phase CBP_(F) and CBP_(R)primers where CBP_(R) is in excess. In a preferred embodiment, the UMIsare present on the rTag prior to writing of the CBP tag. In anotherpreferred embodiment, the rTags are comprised of pseudo-complementarybases (e.g., 2-aminoadenine and 2-thiothymine) to minimize rTagsnon-specifically priming on each other (Lahoud, Georges, et al., 2008.“Properties of Pseudo-Complementary DNA Substituted with Weakly PairingAnalogs of Guanine or Cytosine.” Nucleic Acids Research 36 (22):6999-7008). In an alternate embodiment, the rTag tags are installed onanalytes prior to CBP ISH labeling. Alternatively, both CBP_(F) andCBP_(R) primers can be attached to the macromolecules (e.g., proteins)and act as solid-phase primers in a classical bridge amplification or“cluster amplification” process to effectively transfer, in situ, thegenomic CBP information to the macromolecules (see U.S. Pat. No.7,115,400 B1) within the cell or nuclei. Essentially, a CBP cluster willbe formed at the site of the cell, and if the cells are arrayed on a 2Dsurface such as in a tissue section on a slide, these clusters will growout from the nuclear locations within the cells.

Feasibility of this approach is supported by the following approximatecalculation of the density of recording tag primers within a cell. Theaverage mammalian cell is about 20 um in size with an approximateaverage volume of 3000 um³; within this volume are about 10 billionproteins and assuming each protein is labeled with ten recording tags,this yields 10¹¹ recording tags per cell. This translates to a recordingtag concentration of ˜10 uM, a very high concentration of solid-phaseprimers. Even assuming a 1% efficiency, this is still 100 nMconcentration of primers which is roughly an intra-probe distance of 10nm (Milo, Ron, and Rob Phillips. 2015. Cell Biology by the Numbers.Garland Science).

In some embodiments, amplifying the cell barcodes comprises a)delivering reactive primers that are configured to be covalentlyattached to components of the permeabilized cells, thereby creating aplurality of attached primers; and b) amplifying the cell barcodes usingthe plurality of attached primers, thereby forming amplified cellbarcodes.

In some embodiments, delivery of CBPs to the permeabilized cells and/ornuclei as a part of specific genomic DNA-binding carrier followed byspecific binding to a region in the genomic DNA of the cells and/ornuclei using dCas9 or TALE protein, can be combined with in situ(bridge) amplification of CBPs using reactive primers that delivered tothe cells and/or nuclei and are configured to be covalently attached tocomponents of the permeabilized cells. In these embodiments, there areno partitioning of the cells and/or nuclei into a plurality ofcompartments (compartmentalization step is not present).

In some embodiments, both cDNA from transcribed mRNA and proteins arelabeled with recording tags comprised of a CBP_(F) a primer. In apreferred embodiment, the cDNA recording tag is distinguished from theprotein recording tag by a sequence identifier. This sequence identifiercan be used to enrich and separate the final recording tag NGS libraryelements derived from preparation and processing of cDNAs vs. proteins.

In some embodiments, CBP or cell barcode can comprise either singlestranded or double stranded polynucleotide. In some embodiments, CBP orcell barcode can comprise either DNA or RNA polynucleotide. In someembodiments, CBP comprises a polynucleotide having between 20 and 30nucleotides (nt), between 20 and 40 nt, between 20 and 50 nt, between 20and 100 nt, between 20 and 200 nt, or between 50 and 200 nt. In someembodiments, CBP consists of a polynucleotide having between 20 and 30nt, between 20 and 40 nt, between 20 and 50 nt, between 20 and 100 nt,between 20 and 200 nt, or between 50 and 200 nt. In some embodiments, acell barcode contains between 5 and 20 nt, between 5 and 30 nt, between10 and 20 nt, or between 5 and 100 nt.

Amplified CBPs can be attached to target macromolecules includingmRNA/cDNA and proteins by a variety of methods known in the art.Amplified CBPs can be attached to target macromolecules covalently ornon-covalently, such as via nucleic acid hybridization.

In some embodiments, DNA recording tag stubs (rTags) are joined totarget macromolecules via a chemical bioconjugation reaction (e.g. usinga heterobifunctional agent to attach click-reactive reactive handles toa native biopolymer and enable subsequent click chemistry addition ofdesired tags containing a cognate reactive handle). Exemplary reactionsinclude click chemistry reactions, such as the copper catalyzed reactionof an azide and alkyne to form a triazole (Huisgen 1, 3-dipolarcycloaddition), strain-promoted azide alkyne cycloaddition (SPAAC),reaction of a diene and dienophile (Diels-Alder), strain-promotedalkyne-nitrone cycloaddition, reaction of a strained alkene with anazide, tetrazine or tetrazole, alkene and azide [3+2] cycloaddition,alkene and tetrazine inverse electron demand Diels-Alder (IEDDA)reaction (e.g., m-tetrazine (mTet) or phenyl tetrazine (pTet) andtrans-cyclooctene (TCO); or pTet and an alkene), alkene and tetrazolephotoreaction, Staudinger ligation of azides and phosphines, and variousdisplacement reactions, such as displacement of a leaving group bynucleophilic attack on an electrophilic atom (Horisawa 2014, Knall,Hollauf et al. 2014). In some embodiments, m-tetrazine or phenyltetrazine (pTet) is used in an iEDDA click chemistry reaction. In onecase, a target polypeptide is labeled with a bifunctional clickchemistry reagent, such as alkyne-NHS ester (acetylene-PEG-NHS ester)reagent or alkyne-benzophenone to generate an alkyne-labeledpolypeptide. In some embodiments, an alkyne can also be a strainedalkyne, such as cyclooctynes including Dibenzocyclooctyl (DBCO).

In some embodiments, DNA recording tag stubs (rTags) comprise a firstreactive handle and target macromolecules comprise a second reactivehandle, so that attachment of rTags to the target macromolecules is abioorthogonal reaction. In some embodiments, the first and/or secondreactive handle comprises a bio-orthogonal reactive group (e.g., clickchemistry reagent). In some embodiments, the bio-orthogonal reactivegroup is a reaction partner for an inverse electron demand Diels-Alder(IEDDA) reaction. Some examples of bioorthogonal reactions that can beutilized herein are disclosed, for example, in U.S. Pat. No. 8,236,949B2, U.S. Pat. No. 9,169,283 B2, U.S. Ser. No. 10/611,738 B2, U.S. Ser.No. 10/442,789 B2, and in Fox J M, et al., “General, Divergent Platformfor Diastereoselective Synthesis of trans-Cyclooctenes with HighReactivity and Favorable Physiochemical Properties. Angew Chem Int EdEngl. 2021 Mar. 19”.

In other embodiments, DNA recording tag stubs (rTags) are attached totarget macromolecules indirectly, such as via a linker of variouslengths and flexibility (e.g., PEG linker). In some embodiments, targetmacromolecules are polypeptide that are joined to a bait nucleic acidmolecule which hybridizes with at least a portion of the amplified CBPs.

In a particular embodiment, proteins within permeabilized cells arelabeled with short DNA recording tag stubs (rTags) comprised of a shortCBP amplification primer, such as CBP_(F) or CBP_(R), or combinationthereof (see FIG. 4A-E). These recording tag primers receive CBPinformation from the genomic CBP tag during a CBP amplification reactionsuch as via emulsion PCR, in situ PCR, or bridge amplification. In apreferred embodiment, the recording tags are coupled to proteins usingan amine bioconjugation chemistry using a one- or two-step process. In aone-step process, activated DNA comprised of amine-reactive chemistriessuch as ethynyl moieties or N-hydroxysuccinimide (NHS) moieties areemployed to label lysine amines on proteins; a number of otherbioconjugation methods for lysine labeling are described by Hermanson(Hermanson, Greg. 2013. “Bioconjugate Techniques: Third Edition.”Bioconjugate Techniques: Third Edition, August, 1-1146). In a two-stepprocess, click-enabled heterobifunctional linkers comprised of anamine-reactive component and a click chemistry component are used tofirst activate the lysine amines on the constituent proteins, in asecond step, a DNA tag is covalently attached using click chemistry.Exemplary click chemistries include CuAAC, SPAAC, iEDDA chemistrie(Oliveira, et al., 2017. “Inverse Electron Demand Diels-Alder Reactionsin Chemical Biology.” Chemical Society Reviews 46 (16): 4895-4950).

In some embodiments, barcoded macromolecules are polypeptide analytes;attaching the amplified cell barcodes to the polypeptide analytes can beachieved using different amino acid side-chain specific chemistries. Insome embodiments, chemical coupling between the nucleic acid moleculeand amino acid residues is achieved through amino acid-specific chemicalmodification methods known in the art; for example, lysine residues canbe functionalized with NHS-ester chemistry and cysteine residuesselectively interact with the maleimide group. Examples ofamino-acid-specific chemical functionalization methods are disclosed in,for example, U.S. Ser. No. 10/697,974 B2 and in Zanon PRA, et al.“Profiling the Proteome-Wide Selectivity of Diverse Electrophiles”.ChemRxiv; 2021. DOI: 10.26434/chemrxiv.14186561.v1. In some embodiments,once selective amino acid residues of the polypeptide analytes arefunctionalized, heterobifunctional linkers can be employed to connectnewly installed functional groups on the polypeptide analytes withchemical moieties on the recording tag stubs.

In some embodiments, nucleic acid recording tags are attached tocellular constituents to be barcoded (such as proteins, mRNAs), and thenCBP barcode information is copied from its unique genomic location tothe nucleic acid recording tags using emulsion PCR or bridgeamplification.

In some embodiments, a DNA recording tag stub can be attached to the 5′or 3′ side of cDNA molecules by incorporating the CBP′_(F) or CBP_(F)into the reverse transcription primer or in template switch oligo (TSO),respectively, used in the cDNA “SMART” RT reaction (see, for example,FIG. 7A and FIG. 3 ). At the same time, the CBP can also be incorporatedinto proteins tagged with recording tag comprised of a CBP_(F) primer.

In some embodiments of the disclosed methods, when partitioning of thecells or nuclei having CBPs into a plurality of compartments isemployed, each compartment of the plurality of compartments comprises acompartment barcode configured to be attached to the macromolecules. Inthese embodiments, barcoding of macromolecules with unique cellularbarcodes will improve macromolecule identification by following methods.For example, the cellular proteome can be partitioned into barcodedcompartments. In one embodiment, this partitioning is accomplished usingmethods similar to those disclosed in US20190040382 A1, which isincorporated by reference in its entirety, by direct interaction of aDNA tag labeled polypeptide with the surface of a bead via hybridizationto DNA compartment barcodes attached to the bead. A primer extensionstep transfers information from the bead-linked compartment barcode tothe DNA tag on the polypeptide (see FIG. 13 ). In some embodiments, aprotein molecule (optionally, denatured polypeptide) is labeled with DNAtags by conjugation of the DNA tags to F-amine moieties of the protein'slysine groups or indirectly via click chemistry attachment to aprotein/polypeptide pre-labeled with a reactive click moiety such asalkyne (see FIG. 13 ). The DNA tag-labeled polypeptides are thenpartitioned into compartments comprising compartment tags (e.g., DNAbarcodes bound to beads contained within droplets) (see FIG. 13 ),wherein a compartment tag contains a barcode that identifies eachcompartment. In one embodiment, a single protein/polypeptide molecule isco-encapsulated with a single species of DNA barcodes associated with abead (see FIG. 13 ). In another embodiment, the compartment canconstitute the surface of a bead with attached compartment (bead) tagssimilar to that described in US20190040382 A1, except as applied toproteins rather than DNA. The compartment tag can comprise a barcode(BC) sequence, a universal priming site (U1′), a UMI sequence, and aspacer sequence (Sp). Further, amplified cell barcodes can be attachedto the compartment tag-labeled polypeptides via nucleic acidhybridization and primer extension. In one embodiment, concomitant withor after partitioning, the compartment tags are cleaved from the beadand hybridize to the DNA tags attached to the polypeptide, for examplevia the complementary U1 and U1′ sequences on the DNA tag andcompartment tag, respectively. For partitioning on beads, the DNAtag-labeled protein can be directly hybridized to the compartment tagson the bead surface. The spacer sequence (Sp) on compartment tags (FIG.13 ) can be used for attachment of the amplified cell barcodes.

In some embodiments of the disclosed methods, cleavable linkers are usedfor controlled release of species from beads. Methods for generatingbarcodes that are releasably or reversibly attached to the beads aredescribed, for example, in U.S. Ser. No. 10/428,326 B2, and can beutilized herein. These methods include using thermally cleavable bonds,disulfide bonds, UV sensitive bonds, other non-limiting examples oflabile bonds that may be coupled to a bead, such as an a sulfone linkage(cleavable via a base), ester linkage (cleavable with an acid or abase), a vicinal diol linkage (cleavable via sodium periodate), or aglycosidic linkage (cleavable via an amylase).

The methods disclosed herein allow for generating barcodedmacromolecules from single cells that can be used in a variety ofdownstream applications. Some examples of these applications includenext generation protein analysis (NGPA) and next generation proteinsequencing (NGPS) assays disclosed in US 20190145982 A1, US 20200348308A1 and US 20220049246 A1; and various single cell sequencing techniques,such as scDNA-seq, scRNA-seq, ATAC-seq (see Examples). Barcodedmacromolecules from single cells can be pooled and analyzed together toincrease throughput and efficiency of the analysis. In addition, spatialinformation for single cells can also be preserved by using, forexample, positional barcodes as a part of CBPs.

The methods disclosed herein can be used to generate barcodedmacromolecules from single cells for further analysis, includingdetection, quantitation and/or sequencing, of a plurality of barcodedmacromolecules (e.g., nucleic acids or polypeptides) simultaneously(multiplexing). Multiplexing as used herein refers to analysis of aplurality of barcoded macromolecules in the same assay. The plurality ofbarcoded macromolecules can be derived from the same cell or differentcells. A plurality of barcoded macromolecules suitable for analysisincludes 10 or more macromolecules, 100 or more macromolecules, 500 ormore macromolecules, 1000 or more macromolecules, 10,000 or moremacromolecules, 100,000 or more macromolecules, or more macromolecules.When 100 or more barcoded polypeptides are analyzed simultaneously in asingle assay, it is referred herein as a high-throughput polypeptideanalysis.

In some embodiments, 10 or more macromolecules, 100 or moremacromolecules, 500 or more macromolecules, 1000 or more macromolecules,10,000 or more macromolecules, or 100,000 or more macromolecules arebarcoded by the methods disclosed herein. In some embodiments, 10 ormore different macromolecules, 100 or more different macromolecules, 500or more different macromolecules, 1000 or more different macromolecules,10,000 or more different macromolecules, or 100,000 or more differentmacromolecules are barcoded by the methods disclosed herein.

In some embodiments, barcoded macromolecules produced by the methodsdisclosed herein are polypeptides, and these barcoded polypeptides arefurther analyzed by the following method: (a) contacting the barcodedpolypeptides immobilized on a solid support with a plurality of bindingagents capable of binding to the immobilized barcoded polypeptides; (b)following binding of a binding agent from the plurality of bindingagents to an immobilized barcoded polypeptide, obtaining informationregarding the binding agent, thereby analyzing the immobilized barcodedpolypeptide. In some embodiments, each of the binding agents comprise apolypeptide (engineered binder) or an aptamer. In some embodiments, eachof the binding agents is configured to bind specifically to a portion ofthe barcoded polypeptides. In some embodiments, each of the bindingagents is configured to bind to one or more terminal amino acid residuesof the barcoded polypeptides, or to one or more terminal amino acidresidues modified with a modifying agent. In some embodiments, bindingagents can be developed through directed evolution of affinity scaffoldsusing phage display techniques, as disclosed in U.S. patent applicationSer. No. 17/539,033, filed on Nov. 30, 2021, WO 2022072560 A1, and in USpatent publication US 2022/0283175 A1, incorporated herein. In someembodiments, a plurality of binding agents are a plurality of aptamers,wherein each aptamer from the plurality of aptamers exhibits bindingspecificity toward at least one N-terminal amino acid residue of apolypeptide immobilized on a solid support. Generation of such aptamersare disclosed in US 20210079557 A1, incorporated herein by reference.

In some specific embodiments, the barcoded polypeptides generated by themethods disclosed herein are further analyzed by the following method:(a) contacting a barcoded polypeptide covalently coupled to a solidsupport with a binding agent capable of binding to the polypeptide,wherein the binding agent comprises a nucleic acid coding tag comprisingan encoder sequence that comprises identifying information regarding thebinding agent; (b) transferring the encoder sequence or a complementthereof from the nucleic acid coding tag to the recording tag associatedwith the barcoded polypeptide analyte, wherein the transfer occursthrough a primer extension reaction or ligation; (c) analyzing therecording tag extended after the transfer, wherein analyzing comprises asequencing method, and obtaining the identifying information regardingthe binding agent to provide information regarding the barcodedpolypeptide, thereby analyzing the barcoded polypeptide.

The recited above methods for analysis of barcoded polypeptides provideopportunity for a highly parallel, high-throughput analysis of hundredsand thousands of macromolecules simultaneously in a single assay.

The methods described herein have a broad applicability, including theability to characterize different aspects of individual cells. Oneexample is introducing reagents to individual cells, and characterizingthese cells in response to those reagents. These methods areparticularly suitable for providing characterization of individualcells, cellular components, or macromolecular constituents of the cells,for research, diagnostic and other purposes. One particularly valuableapplication is sequencing and characterization of macromolecularconstituents of a diseased cell, such as a cancer cell. Such cells canhave altered morphological features, gene expression and/or metabolicproperties. Exemplary diseases include cancer, inflammatory disorders,metabolic disorders.

EXEMPLARY EMBODIMENTS

Among the provided embodiments are:

1. A method for barcoding macromolecules from a sample comprising apopulation of cells, the method comprising the following steps:

a. permeabilizing cells, and/or nuclei of the cells, from the populationof cells of the sample;

b. optionally making genomic DNA of the permeabilized cells and/ornuclei at least partially accessible to nucleic acid hybridization;

c. delivering cell barcode probes to the permeabilized cells and/ornuclei of the permeabilized cells, wherein a given cell barcode probecomprises a genome binding element shared among the cell barcode probes,and a cell barcode unique for a given cell barcode probe, and whereinthe genome binding element hybridizes to a region in the genomic DNA,thereby forming a nucleic acid duplex between the genome binding elementand the region of the genomic DNA in the cells and/or nuclei;

d. removing cell barcode probes that are not bound to the genomic DNAfrom the cells and/or nuclei, whereby no more than a defined number ofcopies of the cell barcode probe remain in each cell or nucleus;

e. partitioning the cells and/or nuclei into a plurality ofcompartments;

f. amplifying the cell barcodes within compartments of the plurality ofcompartments, thereby forming amplified cell barcodes within thecompartments; and

g. attaching the amplified cell barcodes to the macromolecules withinthe compartments, thereby forming barcoded macromolecules.

2. The method of embodiment 1, further comprising releasing the barcodedmacromolecules from the compartments.

3. The method of embodiment 1 or embodiment 2, wherein themacromolecules being barcoded are polypeptides, mRNA molecules or cDNAmolecules.

4. The method of any one of the embodiments 1-3, wherein the region inthe genomic DNA is a non-repetitive region.

5. The method of embodiment 4, wherein the non-repetitive region in thegenomic DNA is a non-coding region or a differentially methylatedregion.

6. The method of any one of the embodiments 1-5, wherein the genomebinding element of each cell barcode probe comprises a PCR priming siteadjacent to the cell barcode that is used to amplify the cell barcode atstep (f).

7. The method of any one of the embodiments 1-6, wherein the definednumber of copies is one copy.

8. The method of any one of the embodiments 1-6, wherein the definednumber of copies is two copies.

9. The method of any one of the embodiments 1-8, wherein the sample is aspatial sample, and wherein the sample is dissociated into a pluralityof cells at step (e).

10. The method of embodiment 9, wherein each of the cell barcode probesfurther comprise a positional barcode different for at least some of thecell barcode probes.

11. The method of embodiment 9, wherein the cell barcode probes aredelivered at step (c) from a spatially ordered array.

12. The method of embodiment 9, further comprising, after step (b), (i)delivering a plurality of positional probes to the permeabilized cellsand/or nuclei, wherein a given positional probe comprises a commontargeting element configured to be attached to the macromolecules and apositional barcode different for each positional probes; and (ii)attaching positional probes from the plurality of positional probes tothe macromolecules.

13. The method of embodiment 12, wherein each of the amplified cellbarcodes comprises a common region that is configured to hybridize to aregion in the positional probes; and the method further comprises a stepof performing a primer extension reaction to transfer the amplified cellbarcodes to the positional probes attached to the macromolecules.

14. The method of embodiment 12, wherein the plurality of positionalprobes is delivered from a spatially ordered array.

15. The method of any one of the embodiments 1-9, wherein eachcompartment of the plurality of compartments comprises a compartmentbarcode configured to be attached to the macromolecules.

16. The method of any one of the embodiments 1-15, wherein duringpartitioning the cells and/or nuclei into the plurality of compartmentsat step (e), on average no more than one cell or nucleus comprising acell barcode probe is comprised within a single compartment.

17. The method of any one of the embodiments 1-16, wherein attaching theamplified cell barcodes to the macromolecules within the compartmentscomprises: i) covalently attaching nucleic acid recording tags to themacromolecules or macromolecule derivatives of the cell; and (ii)attaching the amplified cell barcodes to the nucleic acid recordingtags.

18. A method for barcoding macromolecules from a sample comprising apopulation of cells, the method comprising the following steps:

a. permeabilizing cells, and/or nuclei of the cells, from the populationof cells of the sample;

b. delivering reactive primers that are configured to be covalentlyattached to components of the permeabilized cells and/or nuclei, therebycreating a plurality of attached primers;

c. optionally making genomic DNA of the permeabilized cells and/ornuclei at least partially accessible to nucleic acid hybridization;

d. delivering cell barcode probes to the permeabilized cells and/ornuclei of the permeabilized cells, wherein a given cell barcode probecomprises a genome binding element shared among the permeabilized cellsand/or nuclei, and a cell barcode unique for each cell or nucleus, andwherein the genome binding element hybridizes to a region in the genomicDNA, thereby forming a nucleic acid duplex between the genome bindingelement and the region of the genomic DNA in the cells and/or nuclei;

e. removing cell barcode probes that are not bound to the genomic DNAfrom the cells and/or nuclei, whereby no more than a defined number ofcopies of the cell barcode probe remain in each cell or nucleus;

f. amplifying the cell barcodes using the plurality of attached primers,thereby forming amplified cell barcodes within the compartments; and

g. attaching the amplified cell barcodes to the macromolecules withincells, thereby forming barcoded macromolecules.

19. The method of embodiment 18, wherein amplifying the cell barcodes atstep (f) comprises providing conditions for hybridization between thecell barcode probes and the plurality of attached primers.

20. The method of embodiment 18 or embodiment 19, wherein the definednumber of copies is one copy.

21. The method of any one of the embodiments 18-20, wherein themacromolecules being barcoded are polypeptides, mRNA molecules or cDNAmolecules.

22. The method of any one of the embodiments 18-21, wherein the regionin the genomic DNA is a non-repetitive region.

23. The method of embodiment 22, wherein the non-repetitive region inthe genomic DNA is a non-coding region.

24. The method of any one of the embodiments 18-23, wherein each of thecell barcode probes further comprises a positional barcode different forat least some of the cell barcode probes.

25. The method of any one of the embodiments 18-24, wherein the cellbarcode probes are delivered at step (d) from a spatially ordered array.

26. A method for barcoding macromolecules from a sample comprising apopulation of cells, the method comprising the following steps:

a. permeabilizing cells, and/or nuclei of the cells, from the populationof cells of the sample;

b. delivering a specific genomic DNA-binding carrier comprising a cellbarcode probe to the permeabilized cells and/or nuclei, wherein a givencell barcode probe comprises a cell barcode unique for each cell ornucleus, and a priming site, and wherein the specific genomicDNA-binding carrier specifically binds to a region in the genomic DNA ofthe cells and/or nuclei;

c. removing specific genomic DNA-binding carriers that are not bound tothe genomic DNA from the cells and/or nuclei, whereby no more than adefined number of copies of the cell barcode probe remain in each cellor nucleus;

d. amplifying the cell barcodes that were not removed from the cellsand/or nuclei at step (c), thereby forming amplified cell barcodes; and

e. attaching the amplified cell barcodes to the macromolecules, therebyforming barcoded macromolecules.

27. The method of embodiment 26, wherein amplifying the cell barcodescomprises the following steps:

(i) partitioning the cells and/or nuclei into a plurality ofcompartments; and

(ii) amplifying the cell barcodes within compartments of the pluralityof compartments, thereby forming amplified cell barcodes within thecompartments.

In an alternative embodiment, amplifying the cell barcodes comprises: a)delivering reactive primers that are configured to be covalentlyattached to components of the permeabilized cells, thereby creating aplurality of attached primers; and b) amplifying the cell barcodes usingthe plurality of attached primers, thereby forming amplified cellbarcodes.

28. The method of embodiment 26, wherein the specific genomicDNA-binding carrier comprises a catalytically inactive Cas nuclease, aTALE protein or a zinc-finger protein.

29. The method of any one of the embodiments 26-28, wherein the cellbarcode probe is integrated in the genomic DNA of the cells and/ornuclei at step (b).

30. The method of any one of the embodiments 27-29, wherein duringpartitioning the cells and/or nuclei into the plurality of compartments,on average no more than one cell or nucleus comprising a cell barcodeprobe is comprised within a single compartment.

31. The method of embodiment 26 or embodiment 28, wherein at step (d)the cell barcodes are amplified in situ within cells and/or nuclei, andwithout partitioning the cells and/or nuclei into the plurality ofcompartments.

32. The method of any one of the embodiments 26-31, wherein the definednumber of copies is one copy.

33. The method of any one of the embodiments 27-30, further comprisingreleasing the barcoded macromolecules from the compartments.

34. The method of any one of the embodiments 26-33, wherein themacromolecules being barcoded are polypeptides, mRNA molecules or cDNAmolecules.

35. The method of any one of the embodiments 26-34, wherein the regionin the genomic DNA is a non-repetitive region.

36. The method of embodiment 35, wherein the non-repetitive region inthe genomic DNA is a non-coding region.

37. The method of any one of the embodiments 26-36, wherein the genomebinding element of each cell barcode probe comprises a PCR priming siteadjacent to the cell barcode that is used to amplify the cell barcode atstep (d).

38. The method of any one of the embodiments 26-37, wherein the sampleis a spatial sample.

39. The method of any one of the embodiments 26-38, wherein each of thecell barcode probes further comprises a positional barcode different forat least some of the cell barcode probes.

40. The method of any one of the embodiments 27-30, wherein eachcompartment of the plurality of compartments comprises a compartmentbarcode configured to be attached to the macromolecules.

41. The method of any one of the embodiments 27-30, wherein attachingthe amplified cell barcodes to the macromolecules within thecompartments comprises: i) covalently attaching nucleic acid recordingtags to the macromolecules or macromolecule derivatives of the cell; and(ii) attaching the amplified cell barcodes to the nucleic acid recordingtags.

EXAMPLES

The following examples are offered to illustrate but not to limit themethods, compositions, and uses provided herein. Certain aspects of thepresent invention, including, but not limited to, methods of generatingbarcodes, methods of making nucleotide-polypeptide conjugates,embodiments for the Proteocode™ polypeptide sequencing assay, methodsfor attachment of nucleotide-polypeptide conjugates to a solid supportwere disclosed in earlier published application US 2019/0145982 A1, US2020/0348308 A1, US 2020/0348307 A1, US 2021/0208150 A1, U.S. Ser. No.11/427,814 B2, US 2022/0049246 A1, the contents of which areincorporated herein by reference in its entirety.

In the barcoding methods disclosed above and in Examples below, nucleican be isolated from cells and utilized instead of cells; thus, cellbarcode probes can be delivered for association or hybridization with aspecific region (or regions) of gDNA to the permeabilized cells and/orpermeabilized nuclei of the cells. In some embodiments, standard buffersto stabilize the permeabilized nuclei during steps of CBPassociation/hybridization, CBP amplification, compartmentalization canbe employed.

Example 1. Exemplary Samples and Cell Types to be Used in the BarcodingMethods Disclosed Herein

Barcoding methods applied during single cell analysis can be employedusing various cell and tissue types both adherent cells and suspensioncells. Cells can be barcoded in an adherent state and later bedissociated and optionally enriched (e.g., by magnetic-activated cellsorting (MACS), flow sorting, etc.) prior to downstream processing inemulsions. Examples of samples and cell types include: 1) Culturedadherent human cell lines (such as A549, SKBR3) or suspension cells(such as K562, Jurkat); 2) cultured mouse cell lines (such as NIH3T3);3) adherent or suspension blood cells (PMBCs, T-cells, B-cells); 4) cellsuspension from a dissociated tissue sample such as cells prepared fromfixed tissue using vivoPHIX™ Dissociation Protocol (RNAssist); 4)isolated cell nuclei; 5) frozen tissue sections; 6) Formalin-FixedParaffin-Embedded (FFPE) tissue sections.

Example 2. Fixation and Permeabilization of Cells Before Delivering CellBarcode Probes (CBPs) To the Permeabilized Cells Using aFormaldehyde-Based Protocol

Formaldehyde cross-links macromolecules within cells and tissues forfurther analysis. Cells in suspension are washed with phosphate bufferedsaline (PBS) (pH=7.4) three times, and fixed for 10 min at roomtemperature (RT) in paraformaldehyde (1-4% in PBS). After fixation,cells are washed once with PBS supplemented with 10 mM glycine (PFAquenching), and then washed 2 times with PBS, 5 min each at RT. Theamount of paraformaldehyde is optimized for each sample type to provideadequate fixation while minimizing RNA damaging as assessed byevaluating the RNA Integrity Number (RIN) based on comparing 28S to 18SrRNA using known protocols.

For permeabilization, fixed cells are resuspended in 0.5% Triton X-100in PBS and incubated at RT for 5 min. After rinsing with PBS, cells areready for hybridization. Alternatively, fixed and permeabilized cellscan be stored at 4° C. for one day. Other detergents (such as NP40,Tween-20), or alcohol (such as methanol) can also be used forpermeabilization.

Example 3. Fixation and Permeabilization of Cells Before Delivering CBPsto the Permeabilized Cells, Using RNA Preserving Protocols: A DSP-BasedProtocol or an ACME-Based Protocol

Dithio-bis(succinimidyl propionate) (DSP) is a reversible cross-linkerof free amine groups that has previously been shown to preserve tissueintegrity for histology (Attar, M., et al. (2018) A practical solutionfor preserving single cells for RNA sequencing. Sci Rep, 8, 2151). DSPstock solution is prepared by dissolving DSP in anhydrous DMSO to 50mg/mL and stored at −80° C. The DSP stock solution was diluted toworking concentration (1 mg/mL) with PBS immediately before used byadding 490 uL PBS to 10 uL DBS stock dropwise while vortexing. DSPworking solution is filtered using 30 um filter (Miltenyi,Pre-Separation Filters; 30 μm) before use.

Cells or nuclei are centrifuged for 5 min at 200-500 g depending oncell/nuclei size and density, and washed twice with 200 uL 1×PBS. Afterthe final wash, the cell pellet is resuspended gently in 200 uL DSPsolution and incubated at room temperature for 30 min. The reaction isquenched by adding 4.1 uL of 1M Tris-HCl, pH=7.5. After DSP fixation,the cells are permeabilized as described in Example 2.

In addition to DSP, other bifunctional crosslinkers, such as BS(PEG)₅(PEGylated bis(sulfosuccinimidyl)suberate) (Thermo Scientific, A35396),can also be used for cell fixation. Reversible cross-linkers, such asDSP, are useful for preserving RNA integrity by enabling reversal ofdisulfide crosslinks using reducing agents like dithiothreitol (DTT) ortris(2-carboxyethyl)phosphine (TCEP) prior to RNA reverse transcription.

As an alternate to formaldehyde fixation or reversible cross-linkerfixation, an acetic acid/methanol (ACME) protocol can be employed, whichbetter preserves RNA integrity than formaldehyde-based methods(Garcia-Castro, et al., 2021. “ACME Dissociation: A Versatile CellFixation-Dissociation Method for Single-Cell Transcriptomics.” GenomeBiology 22 (1): 89). Namely, cells are fixed and permeabilized byincubating with and ACME solution devoid of methanol (8.5 ml of ACME w/omethanol is comprised of 6.5 ml of 1×PBS buffer supplemented with 1%BSA, 1 ml glycerol, 1 ml of acetic acid, and 100 ul of 7.5% NAC). Thecells are incubated for 20 min. at room temperature on a shaker at 40rpm. After shaking, methanol is added to the cells in ACME buffer to afinal concentration of 15% methanol ACME buffer. Methanol was addedafter initial acid treatment to allow partial fixation in acetic acidprior to permeabilization. After fixation in ACME solution, the cellswere centrifuged at 1000 g for 5 min (4° C.) to remove the ACMEsolution. Cells were resuspended in 1×PBS buffer supplemented with 1%BSA for further processing.

Example 4. Fixation and Permeabilization of Cells Before Delivering CBPsto the Permeabilized Cells, a RNA Preservation Protocol

In some applications, RNA integrity needs to be preserved. For thispurpose, a fixation protocol based on methanol (MeOH) and ammoniumsulfate solutions that precipitates proteins, inhibits enzymaticactivity can be used (Katzenelenbogen, Y., et al. (2020) CoupledscRNA-Seq and Intracellular Protein Activity Reveal an ImmunosuppressiveRole of TREM2 in Cancer. Cell, 182, 872-885 e819). Cells (1×10⁶-5×10⁶)are resuspended in 100 uL of cold PBS supplemented with 0.4 U/uL RNasinPlus RNase Inhibitor (Promega). To avoid cell clumping, 900 uL ofmethanol (pre-chilled to −20° C.) are added dropwise, while gentlymixing to achieve a final concentration of 90% methanol in PBS. Cellsare fixed in methanol for 10 minutes on ice in the dark.

Fixed cells are pelleted at 900 g for 3 minutes right after fixation.Methanol-PBS solution is completely discarded. Cell pellet is washed(not resuspended) twice with ice-cold PBS supplemented with 0.4 U/uLRNasin Plus RNase Inhibitor without breaking the pellet, for completeremoval of methanol leftovers. Cell pellet is resuspended in 100 uL ofenzyme blocking buffer containing ammonium sulfate (Thermo Fisher)solution (0.05 M EDTA (Sigma), 0.8 U/uL RNasin Plus RNase Inhibitor,pH=5.2) and kept on ice for 10 minutes in the dark.

Example 5. In Situ Hybridization (ISH) of CBPs Using Heat and FormamideDenaturation

In situ hybridization of CBPs is performed using an in situhybridization protocol modified from Kapoor et al. (Kapoor and Telford,2004). Cells are fixed and permeabilized according to any one ofExamples 2-4, followed by washing the cells with 1×PBS supplemented with0.1% bovine serum albumin (BSA). After washing, approximately 10⁶ cellsare resuspended in 300 ul of hybridization buffer (70% Formamide, 2×SSC(saline-sodium citrate buffer; Ambion, AM9763), 1% BSA) supplementedwith a cellular barcode probe (CBP) at 50-300 nM concentration (e.g.,CBP_Ch11-344380, SEQ ID NO: 1). The cellular hybridization mix isincubated at 80° C. for 10 min, mixed, and then incubated 2 hours orovernight at 37° C. After the CBP hybridization, excess of the CBP isremoved by washing cells three times in 1 ml wash buffer (2×SSC) at 40°C. for 10 min. Cells are spun down at 400 g between wash steps. Afterthe final wash, cells are resuspended in 1×PBS buffer. A similarprotocol can be applied to fixed/permeabilized tissues on slides.

Exemplar gDNA FISH Probe (iFISH; from Gelali, et al. 2019. “IFISH Is aPublicly Available Resource Enabling Versatile DNA FISH to Study GenomeArchitecture.” Nature Communications 10 (1): 1636).

An exemplar gDNA FISH probe from the iFISH database is a follows: (a)CBP_Ch11-344380; TGGCCAGGAGGAGACTCTTCCAGGTCTCCCTTCTGACACC (SEQ ID NO:1). Target gDNA sequence: chr11, from 344380 to 344419. In a preferredembodiment, the GBS portion of the CBP probe has 35-50 bases of homologywith single copy genomic loci, preferably a non-transcribed andnon-repetitive region.

Another example of an iFISH probe is one containing a PmeI site: (b)Chr7 CBP: AAACCTTGCCAACCATGAGTTTCTGGGACTGACGGTGATG (SEQ ID NO: 2).Target gDNA sequence: chr7, from 63/367,821 to 63/367,861.

Digestion by PmeI enables strand-displacement and optionalligation-based genomic tagging.

Example 6. Adaption of MERFISH for CBP Labeling of gDNA Loci

Using a protocol adapted from Su et al. (Su, et al., 2020. “Genome-ScaleImaging of the 3D Organization and Transcriptional Activity ofChromatin.” Cell 182 (6): 1641-1659.e26), cells mounted on slides arefixed with 4% paraformaldehyde (PFA) in PBS for 10 minutes at roomtemperature and washed 3 times in 1×PBS buffer. Cells are thenpermeabilized by incubating with 0.5% v/v Triton-X100 (Sigma-Aldrich,T8787) in PBS for 10 minutes at room temperature followed by 0.1 Mhydrochloric acid (HCl) treatment for 5 minutes at room temperature. Thecells are then washed again 3 times in 1×PBS buffer. Following washing,cells are incubated in pre-hybridization buffer, consisting of2×saline-sodium citrate buffer (SSC; Ambion, AM9763), 50% formamide(Ambion, AM9342) and 0.1% of Tween-20 (Sigma-Aldrich, P4916) for 30minutes. Next, the cells are incubated in hybridization buffer (2×SSC,50% formamide, 10% dextran sulfate (Sigma-Aldrich, D8906) containing amixture of CBPs at ˜20 nM total concentration with or without 10 μgHuman Cot-1 DNA (ThermoFisher, 15279011). The cells are incubated at−90° C. for 3 minutes and incubated at 47° C. in a humidified chamberfor at least 16 hours. After this incubation step with CBPs, they arewashed in 2×SSC and 40% formamide for 30 minutes and post-fixed with 4%PFA in 2×SSC for 10 minutes at room temperature to lock the CBPs inplace. The cells are subsequently washed 3 times in PBS buffer. Analternate hybridization buffer using ethylene carbonate in lieu offormamide can also employed: this alternate hybridization buffer iscomposed of 2×SSC, 10% (vol/vol) ethylene carbonate (Sigma-Aldrich,E26258), 0.1% (vol/vol) murine RNase inhibitor (NEB), 0.5% (vol/vol)Triton X-100 and 0.4% (vol/vol) Tween-20 in nuclease-free water. The preand post hybridization washes employ a wash buffer comprised of 2×SSC,10% (vol/vol) ethylene carbonate, and 0.5% Tween-20 in nuclease-freewater.

Example 7. ISH of Sample Slides with PNA-DNA Chimeras

A chimeric CBP PNA-DNA probe is designed wherein the GBS portion of theCBP is comprised of PNA and the amplification and barcode portions arecomprised of DNA. Slides are fixed in 4% paraformaldehyde in PBS for 10min at room temperature, washed in 1×PBS, are then dehydrated in 70%,85%, and 100% ethanol for two minutes each in an ice water bath. Theyare then placed in a 2×SSC 70% Formamide solution at 80° C. for 2minutes, followed by an ethanol wash. The CBP PNA-DNA chimeric probe ishybridized to the denatured gDNA in 60% formamide Hyb buffer (60% ofFormamide, 20 mM of Tris-HCl, 200 nM of CBP probe (GBS portion is ˜16-20bases)). This solution is denatured at 85° C. for 5 minutes, then cooleddown to 37° C. before adding 30 μL to each slide. The probes are allowedto hybridize overnight at 37° C., and the slides are then washed in ahigh stringency condition comprised of washing with 2×SSC 70% Formamidesolution for 15 minutes at 37° C., followed by post-hybridizationwashing under in 2×SSC for 4×5 min at 42° C. (Genet, M. D., et al.,2013. Molecular Cytogenetics 6 (1): 42).

Alternatively, fast hybridization buffer containing ethylene carbonateor similar polar aprotic solvents can be employed with the chimericPNA-DNA CBP probe (Matthiesen and Hansen. 2012. PloS One 7 (7): e40675).The chimeric CBP is hybridized directly to the slide without priordenaturation of the gDNA. A fast hybridization buffer is composed of 15%ethylene carbonate, 20 mM of Tris-HCl, 200 nM of the chimeric CBPprobe). This solution is denatured at 85° C. for 5 minutes, then cooleddown to 37° C. before adding 30 μL to each slide. The CBPs are allowedto hybridize overnight at 37° C., and then the slides are washed underhigh stringency condition comprise of washes in 2×SSC and 15% ethylenecarbonate solution for 15 minutes at 37° C., followed bypost-hybridization washing in 2×SSC and 10% ethylene carbonate for 3×5min at 42° C. Ethylene carbonate can also be used for fast hybridizationof standard DNA-based CBPs as well.

Example 8. In Situ Hybridization of CBPs Using Restriction Endonuclease(RE) or Targeted CRISPR/Cas9 Digestion and ExoIII ssDNA Generation

Using an in situ hybridization method modified from the protocoldescribed by Larsson et al (Larsson, et al., 2004. “In Situ GenotypingIndividual DNA Molecules by Target-Primed Rolling-Circle Amplificationof Padlock Probes.” Nature Methods 1 (3): 227-32), cells are preparedfor hybridization with washing in 1×PBS. To initiate restrictiondigestion, a reaction mix of 1×rCutSmart™ Buffer (50 mM PotassiumAcetate, 20 mM Tris-acetate 10 mM Magnesium Acetate, 100 μg/mlRecombinant Albumin (pH 7.9 at 25° C.)) supplemented with 0.5 U/ml MScI(NEB) or PmeI (NEB) is incubated for 37° C. for 30 min with thefixed/permeabilized cellular sample. The CBP is designed adjacent to thetermini created in the gDNA by the described restriction enzymedigestion or Targeted Cas9 digestion as described below in Example 9.After endonuclease digestion, the cells are washed with 1×NEB Buffer 1(10 mM Bis-Tris-Propane-HCl, 10 mM, MgCl2, 1 mM DTT, pH 7 at 25° C.).Next, the gDNA is made single stranded by resuspending the cells in1×NEB Buffer 1 supplemented with 0.2 mg/ml BSA and 10% glycerol andincubating with 0.2 U/ml exonuclease III at 37° C. for 15 min. Afterincubation the slides were rinsed in buffer 1×PBS supplemented with 1 mMEDTA and 0.1% BSA.

After making gDNA regions single stranded within the cells, CBPs arehybridized to the ssDNA within the fixed/permeabilized cells byincubating with 50-300 nM probe concentration in hybridization buffer(30-50% Formamide, 2×SSC, 1% BSA) at 37-50° C. for 1 hr. After probehybridization, excess of probe is removed by washing cells three timesin 1 ml wash buffer (30-50% formamide in 2×SSC) at 37-50° C. for 5 min.Cells are spun down at 400 g between wash steps. Additional morestringent (high formamide and temperature) wash steps can be used asnecessary to reduce background from unbound CBPs. After the final wash,cells are resuspended in 1×PBS buffer.

Example 9. In Situ Hybridization and Ligation or Gap-Fill Ligation ofPadlock CBPs

After linearization of and ssDNA formation within the genomic DNA, thepadlock CBP is annealed and then circularized via ligation. Namely, thepadlock probes are annealed to the fixed and permeabilized cells 100 nMprobe concentration in 6×SSC buffer supplemented with 20% formamide at37° C. for 4 hrs; after hybridization and washing twice with ligationbuffer, the padlock probe arms are ligated by incubation with 0.1 U/mlT4 DNA ligase in ligation buffer (10 mM Tris-acetate pH 7.5, 10 mMmagnesium acetate, 150 mM NaCl, 1 mM ATP, 0.2 mg/ml BSA) at 37° C. for30 min. After ligation, the cells are washed in high formamide buffer toremove non-specifically bound padlock CBPs or unligated CBPs.Circularized CBP probe forms a very stable topological interlocking unitwith the genomic DNA. Alternatively, padlock probes designed with anintervening gap between the two annealed ends can be gap-filled andligated by a cocktail of non-strand displacing polymerase and ligase.Namely, the annealed padlock probe can be gap-filled and ligated usingan enzyme mix containing 0.2 U/μl Phusion High-Fidelity DNA Polymerase(Thermo Fisher Scientific), and 0.5 U/μl Ampligase (Epicentre) in1×Ampligase buffer (20 mM Tris-HCl, 25 mM KCl, 10 mM MgCl₂, 0.5 mM NAD,0.01% Triton X-100) supplemented with 50 μM dNTP, and an additional 25mM KCl. The reactions are incubated at 30 min at 37° C. followed by 45min at 45° C. with a final 2×wash in PBST buffer.

Example 10. CRISPR-dCas9 In Situ Cellular Barcode Tagging of gDNA

A modified protocol from Ishii et al. using RGEN-ISL in situ FISHtechnique is used to label genomic DNA with CBPs (Ishii, et al., 2019.“RNA-Guided Endonuclease—in Situ Labelling (RGEN-ISL): A FastCRISPR/Cas9-Based Method to Label Genomic Sequences in Various Species.”The New Phytologist 222 (3): 1652-61). Namely, single copy genomicregions are targeted with a CRISPR-Cas9 system using either a singlegRNA construct or bipartite gRNA construct. The bipartite gRNA iscomprised of crRNA and tracrRNA that annealed prior to CRISPR-Cas9loading (such as Alt-R@ CRISPR-Cas9, Integrated DNA Technologies).Alternatively, a single gRNA can be employed; the advantage of thebipartite construct is that the tracrRNA portion can be appended withfunctional RNA elements that otherwise may make the gRNA tool long as acontiguous RNA construct.

In the bipartite system, the gRNA is assembled by annealing crRNA withtracerRNA as follows: a mix of 1 μL 100 μM crRNA+1 μL 100 μM CBP-labeledtracrRNA, and 8 μL annealing buffer is denatured for 5 min at 95° C. andslow cooled to room temperature to allow annealing between the crRNAwith tracerRNA. The dCas9 ribonucleoprotein (RNP) complex is assembledby combining 1 μL 10 μM gRNA, 1 μL 6.25 μM dCas9 proteins (D10A and H840A; Novateinbio, PR-137213), 10 μL 10×Cas9 buffer (200 mM Hepes pH 7.5, 1M KCl, 50 mM MgCl₂, 50% (v/v) glycerol, 10% BSA, and 1% Tween-20), 10 μL10 mM DTT, and 80 μL double distilled water. The mix is incubated at 26°C. for 10 min, and stored at 4° C. For each slide processed, 100 μL of1×Cas9 buffer/1 mM DTT is added and incubated for 2 min at roomtemperature. The buffer is removed and 25 μL RNP complex per slide isapplied. The slides are covered with parafilm and kept in a humidchamber at 26° C. for 2-4 h. After incubation, the slides are washed inice-cold 1×PBS for 5 min. To prevent the dissociation of the RNPcomplex, an optional post-fixation step is performed with 4%formaldehyde in 1×PBS for 5 min on ice. Finally, the slides are washedwith 1×PBS for 5 min on ice and dehydrated in ethanol (70, 90, and 96%of ethanol; 2 min each) at room temperature.

Example 11. In Vitro Prime Editing of Fixed/Permeabilized CellsInserting CBPs into gDNA

In a protocol adapted from Anzalone et al., a Prime Editing system isconstructed by assembling a pegRNA with a CRISPR nCas9 (H840A) nickasefused via its C-terminus to an M-MLV RT variant reverse transcriptase(RT) (Anzalone, et al. 2019. “Search-and-Replace Genome Editing withoutDouble-Strand Breaks or Donor DNA.” Nature 576 (7785): 149-57). ThenCas9-RT ribonucleoprotein (RNP) complex is assembled by combining 1 μL10 μM pegRNA, 1 μL 6.25 μM nCas9-RT protein, 1 μL of 0.5 mg/ml FEN1(MCLABS), and 20 μL 5×M-MLV RT buffer (250 mM Tris-Cl pH 8.3, 275 mMKCl, 15 mM MgCl₂, 50 mM DTT, 25% (v/v) glycerol, 5% BSA, and 0.5%Tween-20), 10 μL of 10 mM dNTPs, and 70 μL ddH2O. The mix is incubatedat 37° C. for 5 min, and stored at 4° C. For each slide processed, 100μL of 1×M-MLV RT buffer mix is added and incubated for 2 min at roomtemperature. The buffer is removed and 25 μL nCas9-RT RNP mix is appliedper slide. The slides are covered with parafilm and kept in a humidchamber at 37° C. for 2-4 h. After incubation, the slides are washedwith 1×PBS for 5 min at room temperature.

Example 12. MeFISH Technique to Attach a Single Copy of CBP toMethylated Genomic DNA

Using a protocol adapted from Shiura et al. (Shiura, et al., 2014.“Whole-Mount MeFISH: A Novel Technique for Simultaneous Visualization ofSpecific DNA Methylation and Protein/RNA Expression.” PloS One 9 (4):e95750), permeabilized cells are washed with 2×SSCT (2×SSC with 0.1%Triton X-100) for 10 min, and washed twice with 2×SSCT and 50% formamidefor 10 min. After washing the cells with hybridization buffer (2×SSCT,50% formamide, and 2 mg/ml BSA) for 20 min, the cells are placed in a 10nM solution dipyridyl-labeled CBP probe in hybridization buffer. Thegenomic DNA is denatured by heating at 98° C. for 5 min, andhybridization is performed for ˜16 hrs at room temperature. The cellsare washed three times with 2×SSCT at room temperature for 5 min. TheCBP probe comprised of a GBS sequence containing a bipyridine-attachedadenine derivative, designed to be opposite of a methylated cytosineresidue, is cross-linked to methylated cytosines by incubating infreshly made cross-link solution (25 mM K2OsO4N2H2O, 100 mM Tris-HCl (pH7.4), 1 mM EDTA, 2 M NaCl, and 0.1% Triton X-100) at 30° C. for 10 min.Non-cross-linked probes are removed by denaturation in 90%formamide/2×SSCT followed by washing in PBST (1×Phosphate-BufferedSaline, 0.1% Tween-20).

Example 13. Partitioning the Cells Having Defined Copy Numbers of CBPsinto a Plurality of Compartments, Flow Cytometry-Based Protocol

Cells are partitioned into 96-well or 384-well plates using a FACSinstrument (Cao, J., et al. (2017) Comprehensive single celltranscriptional profiling of a multicellular organism. Science, 357,661-667). First, cells or nuclei are stained with4′,6-diamidino-2-phenylindole (DAPI, Invitrogen) by adding 1.5 uL of 0.1mg/mL DAPI solution to 600 uL cells that are resuspended in 1×PBS with0.5% BSA. Other DNA staining dyes, such as propidium iodide (PI) or SYBRGreen, can also be used instead of DAPI. After staining, the cells aresorted with FACSAria III cell sorter (BD Biosciences) using theoptimized parameters of FSC, SSC, DAPI channels. One DAPI-positivecell/nucleus is placed in each well of 96-well or 384-well plates. Aftersorting single cells, 10 uL of PCR reaction mix that contains 1×Phusionmaster mix (Thermo Scientific), 1 mg/mL BSA, and PCR primers are addedto each well.

Example 14. Partitioning the Cells Having Defined Copy Numbers of CBPsinto a Plurality of Compartments, Droplet-Based Methods

Single cells, together with the aqueous phase containing reagents neededfor the following amplification reaction, are encapsulated into dropletsusing shaking or repetitive pipetting techniques (Redin, D., et al.,(2017) Droplet Barcode Sequencing for targeted linked-read haplotypingof single DNA molecules. Nucleic Acids Res, 45, e125). The aqueous phaseof each assay reaction is consisted of 50 uL PCR reagents containing1×Phusion master mix (Thermo Scientific), 1 mg/mL BSA, and PCR primers.Single cells, together with hybridized barcode template, are also addedto the aqueous phase. The numbers of cells are adjusted based on theanticipated cell doublet rate. The aqueous phase is then added on top of100 uL HFE-7500 oil with 5% (w/v) 008-Flourosurfactant (RanBiotechnologies, MA, USA), and the two phases are emulsified by shakingfor 8 min at 15 Hz in a Qubit™ tube (Life Technologies), using aTissuelyser instrument (Qiagen, MD, USA).

Alternatively, repetitive pipetting can be used to generate droplets.After adding 50 uL aqueous phase to 100 uL oil, a 200 uL pipette settingat 120 uL, is used to mix the aqueous phase and oil. After 40-60 timesof repetitive pipetting, the droplets with encapsulated cells are readyfor PCR reaction.

Commercial droplet generating systems, such as 10×Genomics Chromium,Mission Bio Tapestri, or Dolomite Bio Nadia can also be used toencapsulate cells together with PCR reaction reagents in droplets. Whenusing these commercial droplet generation systems, cell barcode beadsare not needed. Instead, CBPs in the cells will be encapsulated in thedroplets together with the PCR reagents, followed by in-dropletamplification of CBPs, followed by coupling of CBPs to the desiredmacromolecules (such as cell DNA fragments, polypeptides or mRNAmolecules).

In another method, emulsion PCR droplets are created using abead-templated or microparticle-templated emulsion (“dropsicles”)process as described in Hatori et al. and Wu et al. (Hatori, et al.,2018. “Particle-Templated Emulsification for Microfluidics-Free DigitalBiology.” Analytical Chemistry 90 (16): 9813-20), (Wu, et al., 2020.“Monodisperse Drops Templated by 3D-Structured Microparticles.” ScienceAdvances 6 (45): eabb9023), and in US patent application US20200261879A1. In US20200261879 A1, the use of bead-templated emulsion incombination with cell encapsulation is described. The beads are in atleast ten-fold excess over cells to ensure single cell loading perdroplet. The bead size is larger than the average cell size to favorcompartmentalization of cells along with beads in a compartment wherethe bead serves primarily a templating vehicle. These droplets can beloaded with PCR reagents to enable an ePCR reaction.

Alternatively, emulsion PCR droplets are created directly from fixedcells, and particularly fixed cells that have been intracellhydrogelated in which the interior of the cell has been filled withcross-linked hydrogel polymer (Lin, et al., 2019. “IntracellularHydrogelation Preserves Fluid and Functional Cell Membrane Interfacesfor Biological Interactions.” Nature Communications 10 (1): 1057). Theelastic modulus of the cell renders is sufficiently robust to enabletemplated emulsions directly from the cell itself. Once in the droplet,the hydrogel matrix can be dissociated by using a cleavable crosslinkersuch as a disulfide containing crosslinker. In brief, using a protocoladapted from Lin et al., hydrogelated cells are generated post-genomicCBP labeling and rTagging process, by incubating with cells with agelation mix comprising a 1 wt % of the photo crosslinker2-hydroxy-4′-(2-hydroxyethoxy)-2-methylpropiophenone (Irgacure D-2959;Sigma-Aldrich), and the dissolvable polymer poly(ethyleneglycol)-SS-diacrylate (the PEGSSDA reagent; Advanced Biomatrix, CA)ranging from 4 to 40 wt % in 10 mM phosphate buffer. Cells in suspensionis pelleted at 200 g and resuspended in designated gelation mix. Forcross-linking adherent cells, cells grown on a tissue culture plate orslides are washed with PBS and immersed in the designated gelation mix.The suspension cells are pelleted at 200×g and resuspended in PBS on atissue culture plate, whereas adherent cells are washed with PBS twice.The tissue culture plates are then placed in an ice bath, and the cellsare crosslinked with 365 nm UV wavelength for 10 min using a UV lamp(UVP UVLMS-38 EL Series) placed 2 in. above the tissue culture plate.The resulting cells are washed twice in PBS for further processing.

After templated emulsion generation, the hydrogel is dissolved byincubation in 1 mM DTT at 30° C. for 10 min. After cell hydrogelation,100 ul of hydrogelated cells (per volume) are combined with 200 ul 2×PCRMaster Mix, 18 ul of 1 uM CBP_(F) and 18 ul 10 uM CBP_(R) primer, 8 ul10% TX-100, and 38 ul water. The mix is incubated at room temperaturefor 15 min under gentle agitation (10 rpm) using a tube rotator toensure homogenous distribution of the PCR components within the cell.The disperse phase is centrifuged at 600 g for 1 min and the supernatantis removed. A volume of 200 μL 2% fluorosurfactant in HFE-7500 oil(008-Fluoro-surfactant, RAN Biotechnologies) is added to the tube as theinsoluble continuous phase for emulsification. The hydrogelated cellpellet is dislodged by pipetting or tapping/flicking the tube. Thesample is then vortexed at 2000-3000 rpm for 30 sec. The emulsion isallowed to settle for 1 min. A volume of 100 μL of the bottom oil phaseis removed and replaced with an equal volume of fresh 2%fluorosurfactant in HFE oil. The tube is gently inverted several timesto mix. This step is repeated 3-5× or until small satellite dropletshave been removed. After emulsification, the hydrogel within the cellsis dissolved by exchanging the 2% fluorosurfactant in oil mix withfluorosurfactant pre-saturated with DTT effectively dissolving thehydrogel by reducing the disulfide bonds of the hydrogel from thePEGSSDA reagent. This hydrogel dissolution should improve the ePCRefficiency.

Extraction of macromolecules after ePCR is accomplished by adding 1% SDSin TK buffer (20 mM Tris-HCL, pH 7.5, 60 mM KCl, 10 mM DTT) to cellsextracted from the emulsion and incubating at 95° C. for 5 min.Cysteines are alkylated by incubating with 40 mM iodoacetamide for 1 hat 37° C. in dark. Samples are diluted 10-fold in TK buffer andincubated with 20 ng/μL porcine trypsin (1:50 trypsin:protein ratio) for3 h at 37° C. Following treatment, lysate is again centrifuged andresuspended in 1×TK buffer for downstream processing and librarypreparation.

Example 15. Amplification of CBPs within Compartments and Coupling ofAmplified CBPs to DNA Fragments

In this Example, the aqueous phase enclosed in the droplets comprises1×Phusion High-Fidelity PCR Master Mix (Thermo Fisher) and 1.0 mg/mLrecombinant BSA (New England Biolabs). A pair of barcode primers(CBP_(F) at 1 uM and CBP_(R) at 0.05 uM) are designed to amplify thecell barcode sequence within the droplet, as shown in FIG. 3 . A singleprimer (GSP-R at 0.2 uM) is used to linearly amplify the cell DNAfragments. There is a 10 bp overlap region between CBP_(R) and 5′-end ofcell DNA fragment to facilitate the coupling reaction to link twofragments together (FIG. 3 ). Because all copies of the cell barcode(CBC) present in CBP in the same droplet are originated from a singlebarcode sequence, after coupling reaction all cell DNA fragments fromthe same droplet representing a single cell will be labeled with thesame CBC. With a large pool of degenerate CBC sequences (4¹⁴=2.68*10⁸),the chances that cell DNA fragments from different droplets receive thesame CBC sequences are low.

The PCR program is separated into two stages. The first stage uses ahigher annealing temperature (65° C.) to amplify both the cell barcodeand cell DNA fragments. The second stage uses a lower annealingtemperature (48° C.) to allow the 10 bp overlap region between CBP_(R)and 5′-end cell DNA fragment to anneal and extend to form couplingproducts. The complete PCR program is as following: 98° C. initialdenaturation for 1 min, 22 cycles of stage one (98° C. for 10 sec, 65°C. for 40 sec, 72° C. for 30 sec), 5 cycles of stage two (98° C. for 10sec, 48° C. for 2 min, 72° C. for 40 sec), and a final extension at 72°C. for 2 min.

After the completion of PCR amplification and coupling reaction, 15 uLof Ethylenediaminetetraacetic acid (EDTA, 100 mM) (Invitrogen) is addedand the entire emulsion reaction is transferred to a DNA LoBind tube(Eppendorf). To break the droplets and recover the coupling product, 200uL of 1H,1H,2H,2H-Perfluoro-1-octanol (Sigma) is added. The mixture isthen vortexed for 10 s at maximum speed, followed by centrifuging for 5min at 20,000×g. After phase separation, the aqueous phase on the topthat contains the coupling product is transferred to a fresh LoBind tubefor downstream purification (Redin, D., et al., (2017) Droplet BarcodeSequencing for targeted linked-read haplotyping of single DNA molecules.Nucleic Acids Res, 45, e125).

Example 16. In Silico Merging Macromolecules from the Same DropletBarcoded by Two or More Barcode Sequences for Further Analysis

In some embodiments of the disclosed barcoding methods, after removingcell barcode probes (CBPs) that are not bound to the genomic DNA (gDNA)from the cells, two or more CBPs remain bound to gDNA inside cells,which results in two or more cell barcode sequences being encapsulatedand amplified in the same droplet, and subsequently used to label thedesired macromolecules originated from the same cell. To avoidmis-interpretating these barcodes to multiple cells, these barcodes needto be merged in silico. One strategy to accomplish this is to utilizeUnique Molecular Identifier (UMI) sequences incorporated in themacromolecules, such as cell DNA fragments. The cell barcodes from thesame droplets will share UMI sequences at a rate exceeding that may beexpected by chance (Lareau, C. A., et al. (2019) Droplet-basedcombinatorial indexing for massive-scale single cell chromatinaccessibility. Nat Biotechnol, 37, 916-924; Lareau, C. A., et al.,(2020) Inference and effects of barcode multiplets in droplet-basedsingle cell assays. Nat Commun, 11, 866). For each pair of cellbarcodes, the Jaccard index is computed over the UMI sequences,providing a measure of how similar the UMI sequences are for any pair ofcell barcodes (FIG. 11A). From these pairwise Jaccard index statistics,a knee plot is generated to determine pairs that are likely to haveoriginated from the same droplet, and a Jaccard index cutoff value canbe used to determine barcode pairs that need to be merged (FIG. 11B).

Example 17. Amplification of Padlock CBP by Rolling-Circle Amplification(RCA)

A padlock CBPs are circularized oligonucleotides (Nilsson, M. 2006. Lockand roll: single-molecule genotyping in situ using padlock probes androlling-circle amplification. Histochem. Cell Biol. 126: 159-164).Before circularizing, linear CBPs are designed to include thecomplementary nucleotide sequences of the target sequence of gDNA inboth terminal regions, and unique cell barcodes in the middle region.When the linear CBP is in close proximity with the target sequence ofgDNA, the terminal regions of the CBP hybridize with the target sequenceof gDNA and form the double strands, while the middle region remains asa single strand without hybridization. After the hybridization, the twoends can be connected by DNA ligase to form a circularizedoligonucleotide as a padlock for the target gDNA sequence (FIG. 6 ).Next, DNA polymerase having strong strand displacement activity can beutilized amplify the cell barcode sequence of the padlock CBP byrolling-circle amplification (RCA). Examples of such DNA polymeraseenzymes include, but not limited to, Klenow exo-, Bsu large fragment,phi29 the large fragment of Bst DNA polymerase, an engineeredthermostable polymerase having a strong strand displacement activity,such as, for example, Taq DNA polymerase mutant (Ignatov K B, et al., Astrong strand displacement activity of thermostable DNA polymerasemarkedly improves the results of DNA amplification. Biotechniques. 2014Aug. 1; 57(2):81-7).

Example 18. In Situ cDNA Synthesis and Crosslinking

Using a protocol adapted from Lee et al. (Lee, Je Hyuk, et al., 2014.“Highly Multiplexed Subcellular RNA Sequencing in Situ.” Science 343(6177): 1360-63), the mRNA within fixed and permeabilized cells are insitu reverse transcribed using the following protocol: a 200 uL mixturecontaining 4,000 U M-MuLV reverse transcriptase (Enzymatics), 250 uMdNTP (Enzymatics), 40 uM aminoallyl dUTP (Anaspec), 50 U RNase inhibitor(Enzymatics), and 100 pmol phosphorylated CBP_(F)-oligo dT primerprepared on ice is added to cells at 25° C. for 10 minutes. Theconcentration of aminoallyl dUTP is varied depending the cell type andthe application. Generally, a high incorporation rate of aminoallyl dUTPresults in better cross-linking and reduced cDNA diffusion but a loweramplicon density. The sample is then incubated overnight in a humidified37° C. chamber. The sample is washed using 1×PBS and cross-linked usingBS(PEG) 9 (Thermo Scientific), diluted to 50 mM in PBS, for 1 hour at25° C. 1 M Tris (G Biosciences) is added to quench the reaction for 30minutes at 25° C. A mixture of DNase-free RNases (Roche Diagnostics) andRNase H (Enzymatics) is added to degrade residual RNA for 1 hour at 37°C.

Example 19. RCA Pre-Amplification of CBP

Using a protocol adapted from Lee et al., 2014, an optional rollingcircle amplification (RCA) reaction can be used to pre-amplify the CBPtags within the nucleus prior to emulsion or dropletcompartmentalization followed by emulsion PCR. The initial CBP pre-RCAprobe is comprised of a 5′ GBS and a 3′ CBP_(F) primer sequence that cananneal to a pre-circularized cellular barcode probe via a complementaryCBP_(F) sequence. An architecture for the primer suitable for thisprocess is shown in FIG. 7C except the barcodes are inserted during theRCA step. The annealing reaction is initiated by adding 200 uL mixturecontaining 100 nM pre-circularized CBP construct in 2×SSC and 30%formrnamide for 15 minutes at 60° C. The sample is washed using 2×SSC,and a 200 uL RCA amplification mixture containing 500 U Phi29 DNApolymerase (Enzymatics), 250 uM dNTP is added. The sample is incubatedin a dry 30° C. chamber overnight and cross-linked using BS(PEG) 9diluted to 50 mM in PBS for 1 hour at 25° C. After a rinse with PBS, 1 MTris is added to quench the reaction for 30 minutes. At this point, thesample can be stored in nuclease-free 1×PBS at 4° C.

Example 20. Attaching Positional Barcodes to Macromolecules (Such asPolypeptides) to Preserve Spatial Information in a Spatial Sample (e.g.,Tissue Section)

Positional barcodes are introduced into a mounted tissue section (freshfrozen or paraffin embedded) by overlaying and assembling DNA barcodedbeads used as spatial probes on the surface of the mounted tissuesection on the slide (Fischer et al., CSH Protoc (2008) pdb prot4991;Fischer et al., CSH Protoc (2008) pdb top36; Fischer et al., CSH Protoc.(2008) pdb.prot4988). Fresh-frozen tissue cryo-sections (e.g., about 5to about 100 μm thickness, such as 10 μm thickness) are transferred ontothe slide surface and undergo 4% formaldehyde fixation for about 20minutes. The tissue section slides are dried with forced nitrogen airbefore the barcode bead overlay. Barcoded beads are brought into contactwith the tissue section by incubating beads with the slides and spinningdown the beads to form a monolayer on the slide surface. The tissuesurface is covered with beads attached non-specifically to the tissuesurface through adhesive forces such as charge interactions, DNAhybridization, or reversible chemical coupling. In another embodiment,the beads are embedded in a hydrogel coated over the tissue sectionsurface. In one embodiment, the beads are porous to accommodate a higherloading of barcodes on a bead (a porous 5 um bead can be loaded with>10¹⁰ DNA barcodes, e.g. Daisogel SP-2000-5 porous silica beads).Positional barcodes are attached to the beads via a photocleavablelinker enabling easy removal and subsequent diffusive transfer of thebarcodes to the tissue section. Positional barcodes can be released byenzymatic, chemical, or photo-cleavage of a cleavable linker. Thesebarcodes permeate the tissue slice and anneal to the DNA stubs (e.g.,recording tags) attached to polypeptides within the tissue slice. Apolymerase extension step is used to write the positional barcodes tothe DNA recording tags on the proteins, generating an extended recordingtag.

In alternative embodiments, positional barcodes are provided as a partof the CBPs (see, for example, FIG. 4A, where exemplary CBS comprisesSpBC).

Further details for attaching positional barcodes to macromolecules areprovided as follows:

Tissue Section Permeabilization

For fresh frozen samples, the tissue section is permeabilized usingstandard methods such a 0.1%-1% TX-100 incubation prior to chemicalactivation of protein molecules (Fischer et al., CSH Protoc (2008) pdbtop36). For FFPE tissue sections, the embedding media is removed (e.g.,dewaxed in the case of paraffin), and the sections are permeabilizedusing standard methods (Ramos-Vera et al., J Vet Diagn Invest. (2008)20(4):393-413). Standard conditions for tissue permeabilization includeincubation in 0.1%-1% TX-100 or NP-40 for 10-30 min at 0.1 to 1%.Tween-20, Saponin, Digitonin can also be used at 0.2%-0.5% for 10-30 min(Fischer et al., CSH Protoc (2008) pdb top36).

Chemical Activation and DNA Tagging

After tissue section permeabilization and protein denaturation, in apreferred embodiment, proteins are chemically activated by incubationwith an amine bifunctional bioconjugation reagent such asmethyltetrazine-sulfo-NHS ester (Click Chemistry Tools); otherbifunctional amine reactive bioconjugation reagents can also be employed(Hermanson, Greg. 2013. “Bioconjugate Techniques: Third Edition.”Bioconjugate Techniques: Third Edition, August, 1-1146). The density ofDNA tagging can be controlled by titrating in non-activated aminemodifying reagent such as mPEG-NHS ester. An exemplar activationcondition includes incubating slides with 1 mM NHS-mTet for 30 min inPBS buffer (pH 7.4) to label epsilon-amine on lysines. Wash 3× in PBSsupplemented with 5 mM ethanolamine for 10 min each to quench reaction.After activation and washing, a common DNA tag (comprising a suitablearchitecture for a recording tag) containing an iEDDA coupling labelsuch as trans-cyclooctene (TCO), norbornene, or vinyl boronic acid isincubated with the tissue section to “click on” the DNA tags to the mTetmoieties on the activated protein molecules (Knall et al., TetrahedronLett (2014) 55(34): 4763-4766). An exemplar coupling condition includesincubating the slide with 1 mM TCO-DNA stub for 1 h in PBS buffer (pH7.4). Excess TCO-DNA is washed away using PBS buffer washes. The DNAstub is comprised of a priming sequence present on the final amplifiedCBP sequence enabling primer extension to copy the CBP sequence to eachDNA-tagged protein analyte within the cell or cellular compartment. Inaddition, the DNA stub may be comprised of a amplification region, abarcode region (e.g. sample barcode), and a primer region capable ofannealing to the CBP to facilitate a primer extension step (Fig. ?).

DNA Barcoded Bead Distribution Over Tissue Section.

In a preferred embodiment, DNA barcoded beads are generated through asplit-pool synthesis strategy described in (Klein et al., Lab Chip(2017) 17(15): 2540-2541) or in (Delley and Abate. 2021. “ModularBarcode Beads for Microfluidic Single Cell Genomics.” Scientific Reports11 (1): 10857). Each bead has a single population of positionalbarcodes. In one embodiment, the beads are 0.5-10 um in diameter andcontain a positional barcode flanked by an upstream spacer sequence anda downstream primer extension sequence complementary to the DNA tagsequence attached to the proteins. In a preferred embodiment, the DNAbarcodes are attached to the bead with a photo-cleavable linker, such asPC linker (PC Linker-CE Phosphoramidite, Glenn Research). In anotherembodiment, tissue section slides are assembled in a capillary gapflow-cell (˜50 um gap) such as the Te-Flow system from Tecan (Gunderson,Methods Mol Biol (2009) 529: 197-213). This provides a format for easilyexchanging solutions on the slide surface.

In one embodiment, DNA barcoded beads are distributed across the surfaceof the tissue section, using the capillary gap flow cell system. The DNAbarcode beads contain complementary sequences to the DNA tags on theproteins. This creates a “stickiness” of the barcoded beads to thesurface of the tissue section with exposed DNA tags. In anotherembodiment, the beads are 0.5-10 um in diameter and contain both DNAbarcodes and free amines on their surface. These free amine groupsenhance adhesion to tissue surfaces since most tissues are slightlynegatively charged (this is the mode to mount tissue slices onpositively-charged slides for IHC). The barcoded beads can be covalentlycross-linked to the tissue using standard fixation chemistry withglutaraldehyde.

Transferring Positional Barcodes from Beads to DNA Tagged Proteins

After assembling barcode beads on the surface of the tissue section, thepositional barcodes are photo-cleaved from the bead (via long wavelengthUV exposure, e.g. 365 nm UV). A majority of linkages are cleaved, butnot all, since photo-cleavage is generally only 70-90% efficient and canbe adjusted by UV intensity and exposure time (3-100 mW/cm2 @ 340-365 nmfor 1-60 min) (Bai et al., Proc Natl Acad Sci USA 100(2): 409-413). Thecleaved positional barcodes diffuse into the tissue section andhybridize with their complement on DNA tags (e.g., recording tags)previously attached to proteins. After incubation for about 30 min, thetissue section is exposed to a polymerase extension mix to transferpositional barcode information from the hybridized positional barcode tothe polypeptide DNA recording tag.

Example 21. Preparing Spatially Ordered Array of Positional BarcodeProbes (PBPs) on Glass Slides

The protocol is adapted from (Srivatsan, S. R., et al. (2021)Embryo-scale, single-cell spatial transcriptomics. Science, 373,111-117) with modifications. A thin membrane of dried agarose isfabricated on the surface of microscope slides (Superfrost Plus,Thermofisher) to absorb and retain an array of spotted PBPs (see belowfor PBP spotting procedure). Nuclease-free agarose is prepared by adding3% w/v low melting temperature agarose powder (SeaPlaque, Lonza, Bend,Oreg.) to deionized water containing 0.1% v/v diethyl pyrocarbonate. Themixture is incubated for 2 hr at room temperature, and autoclaved for 15min. The uniform thickness of the layer of agarose across the slidesurface is patterned using spacers of two stacked 22×22 mm, number onethickness (0.15±0.02 mm each) coverslips overhanging either end of theslide. Molding of the agarose is performed by pipetting a 300 uL volumeof heated agarose solution into the center of the slide and slowlyplacing a second slide onto the agarose solution avoiding the formationof bubbles. The agarose is solidified by putting on ice for 30-60 min.The resulting thin layer of agarose gel is dried onto the bottom slideovernight in a biosafety cabinet. All agarose slides are UV-treated for20-30 min prior to spotting to further protect against nucleaseactivity.

The space-grid array of PBPs is spotted onto agarose-coated slides usinga QArray2 microarray scanner (Genetix, New Milton, Hampshire, GB). Aseries of 384-well high sample recovery plates (Molecular Devices, SanJose, Calif., X7020) is prepared containing PBPs (Integrated DNATechnologies, Coralville, Iowa), and 0.5% v/v glycerol to achieve thepredetermined PBP layout. In an 18 mm by 1.8 mm area, 7,056 of uniquePBP can be spotted (mean radius of 73.2±14.1 um; mean spot-to-spotcenter distance of 222±7.5 um).

Example 22. Barcoding Macromolecules with Positional Barcodes in TissueSections to Record Spatial Information

Single-stranded DNA (ssDNA) can label the nuclei of permeabilized cells(Srivatsan, S. R., et al. (2020) Massively multiplex chemicaltranscriptomics at single-cell resolution. Science, 367, 45-51). PBPsare prepared as in Example 21 and transferred in their arrayed patternfrom the space-grid slides to fresh-frozen sections by diffusion throughcell permeabilization buffer. First, the tissue section slide is placedso that it rested (tissue facing up) with the tissue section between twotransfer clips. Subsequently, 500 μL of nuclei permeabilization buffer[10 mM Tris/HCl pH 7.4, 10 mM NaCl, 3 mM MgCl2 with 1% v/v superaseinhibitor (Invitrogen) and 0.1% v/v IGEPAL CA-630 (Sigma Aldrich)] ispipetted gently onto the tissue section. A space-grid array slide isthen positioned (agarose surface facing the tissue section) so that thearrayed PBPs are aligned between the two transfer clips and spanned thetissue section's extent. After transferring PBPs to cell nuclei, cellsof the tissue section are scraped using a cell scraper (Fisherbrand,GDPC240) into a 4% paraformaldehyde fixing solution. After fixation for15 minutes on ice, cells are spun down in 1.5 mL tubes in a chilledbenchtop centrifuge at 800 g for 10 minutes. The supernatant in eachtube is removed and cells are pooled in 1 mL of NSB [Nuclei SuspensionBuffer (10 mM Tris/HCl pH 7.4, 10 mM NaCl, 3 mM MgCl2) with 1% v/vsuperase inhibitor (Invitrogen) and 1% v/v BSA (New England Biolabs)]and subjected to barcode amplification and macromolecule labeling asdescribed in Examples 15 and 20.

Example 23. Next Generation Protein Analysis (NGPA) and Next GenerationProtein Sequencing (NGPS) Assays

Macromolecules barcoded with CBPs can be pooled together from individualcells and further analyzed by a variety of methods. For peptidemacromolecules, either NGPA or NGPS assays can be used (see US20190145982 A1).

In these assays, peptide molecules are attached to nucleic acidrecording tags (each recording tag includes a cellular barcode from CBPand, optionally, a positional barcode) and recording tag-peptideconjugates are immobilized on a solid support, such as beads. Forexample, recording tag-peptide conjugates are joined to immobilizedbead-attached capture DNAs via nucleic acid hybridization, as describedin US 2020/0348308 A1. Briefly, conjugates (20 nM) are annealed to thecapture DNAs attached to beads in 5×SSC, 0.02% SDS, and incubated for 30minutes at 37° C. The beads are washed once with PBST and resuspended in1×Quick ligation solution (New England Biolabs, USA) with T4 DNA ligase.After a 30-minute incubation at 25° C., and the beads are washed withPBST, two times of 0.1M NaOH+0.1% Tween-20 and twice of PBST.

Immobilized recording tag-peptide conjugates are analyzed by incubationwith one or more binding agents that are capable of specifically bindingto the peptide (or a component of the peptide, such as one or more aminoacid residues, or post-translational modification of the peptide) of oneof recording tag-peptide conjugates. Each binding agent is conjugatedwith a nucleic acid coding tag that comprises barcode comprisingidentifying information regarding the associated binding agent. Ifaffinity of the binding agent to the immobilized peptide is strongenough (typically, Kd should be less than 500 nM, and preferably, lessthan 200 nM), the coding tag associated with the binding agent and therecording tag associated with the peptide form hybridization complex viahybridization of the corresponding spacer regions to allow transfer ofidentifying information from the coding tag to the recording tag via aprimer extension reaction (encoding reaction), generating extendedrecording tag. This can be performed in parallel for multipleimmobilized peptides and for multiple binding agents. If more than onebinding agent bind specifically to the peptide, history of bindingevents is recorded in the extended recording tag associated with thepeptide. Sequencing of extended recording tags after one or moreencoding cycles is used to identify binding agent(s) that was(were)bound to the immobilized peptide. At the same time, estimating fractionsof the recording tags being extended (encoded) during primer extensionreaction provides estimate of efficiency of the encoding reaction, whichdirectly correlates with binding affinity of the binder to the peptide.

In NGPA assay, specific antibodies recognizing peptide epitopes areemployed as binding agents, which provides high throughput proteincharacterization based on epitope mapping (by associating identifyinginformation of the binding agents having known specificities extractedfrom the extended recording tags with sequences of proteins). In NGPSassay, a set of binding agents (5-20 binding agents) are employed thatspecifically recognize different modified N-terminal amino acid (NTAA)residues of peptides. After one cycle of binding and encoding, themodified NTAA residues are removed (chemically or enzymatically),exposing new NTAA residues of peptides. New NTAA residues are modifiedwith a functionalizing reagent, followed by incubating modifiedimmobilized peptides with the set of binding agents, and the secondcycle of binding and encoding occurs. Thus, full cycle of NGPS consistsof NTAA modification, binding, encoding and NTAA cleavage. This cyclecan be repeated 2-15 times, which results in generation of long extendedrecording tags associated with immobilized peptides and bearingidentifying information regarding all binding agents that were bound tothe particular peptide. Since specificity of the binding agents isknown, it can be used to decode sequence of the peptide in highthroughput manner.

Example 24. Single-Cell Protein Detection Based on NGPA Assay UsingIn-Droplet Amplified Cell Barcodes

Cells are fixed and permeabilized as described in Example 2. Recordingtags (R-tag) are attached on cellular proteins via a one-pot, two-stepreaction by combining cell samples with methyltetrazine-activated DNA(MTZ-DNA) oligonucleotides and the amine-reactive cross-linkerNHS-trans-cyclooctene (NHS-TCO) (see US20190276818 A1, incorporatedherein, and Gehring, J., et al. (2020) Highly multiplexed single-cellRNA-seq by DNA oligonucleotide tagging of cellular proteins. NatBiotechnol, 38, 35-38). The cells are then undergone two cycles of NGPAreaction each consisted of six steps: 1) incubate cells for 30 min atroom temperature with antibody mix conjugated with coding tag (C-tag).2) wash cells with PBST. 3) Information transfer from C-tag to R-tagusing an extension mix containing 0.2 U/uL Klenow Exo- and 0.125 mMdNTP. The extension reaction was conducted at 37° C. for 10 min. 4) washcells with PBST, 5) SHT buffer (1% Tween20, 0.1M NaOH) was applied todenature double stranded DNA formed during extension and stripantibodies off their respective target proteins. 6) wash cells two moretimes with PBST. The antibody mixtures were consisted ofC-tag-conjugated antibodies targeting different proteins. To distinguishdifferent protein targets, C-tags on different antibodies were assignedwith different barcode sequences (antibody barcodes). Two cycles ofsequential NGPA reactions are used to improve the specificity.

After the NGPA reaction, C-tag identifying information from cycle 1 andcycle 2 antibodies are recorded on R-tag to form a composite oligo(R-C1-C2) that reflects both the identity and quantity of the proteintargets. These composite oligos are still confined in fixed cellsbecause R-tag are anchored on the cellular proteins. The cells are thenincubated with CBPs as described in any one of Examples 5, 6, 8-12 toincorporate 1-2 unique CBPs into each individual cell followed byencapsulating cells with CBPs into droplets for CBP amplification andR-C1-C2 barcoding.

Example 25. Single-Cell ATAC-Seq Using In-Droplet Amplified CellBarcodes

The first step of single-cell ATAC-seq protocol is to prepare nucleiaccording to Corces, M. R., et al. (2017) An improved ATAC-seq protocolreduces background and enables interrogation of frozen tissues. NatMethods, 14, 959-962. Cells grown in tissue culture are pretreated with200 U/ml DNase (Worthington) for 30 min at 37° C. to removefree-floating DNA in the media. The cells are then collected andresuspended in cold PBS. After the cells are counted, 50,000 cells areresuspended in 1 ml of cold ATAC-seq resuspension buffer (RSB; 10 mMTris-HCl pH 7.4, 10 mM NaCl, and 3 mM MgCl₂ in water). Cells arecentrifuged at 500 g for 5 min in a pre-chilled (4° C.) fixed-anglecentrifuge. After removing supernatant, cell pellets are resuspended in50 μl of ATAC-seq RSB containing 0.1% NP40, 0.1% Tween-20, and 0.01%digitonin. The cell lysis reaction is carried out on ice for 3 min.After lysis, 1 ml of ATAC-seq RSB containing 0.1% Tween-20 (withoutNP-40 or digitonin) is added, and the tubes are inverted to mix. Nucleiare then centrifuged for 10 min at 500 g in a pre-chilled (4° C.)fixed-angle centrifuge. For transposition reaction, nuclei areresuspended in 50 μl of transposition mix (25 μl 2×TD buffer, 2.5 μltransposase (Illumina), 16.5 μl PBS, 0.5 μl 1% digitonin, 0.5 μl 10%Tween-20, and 5 μl water) and incubated at 37° C. for 30 min.

The tagmented nuclei are then labeled with CRISPR/CAS CBP as describedin Example 10 to assign 1-2 cell barcodes to individual cell nuclei.Then, the nuclei are encapsulated in droplets together with PCR reagentsfor cell barcode amplification and ATAC fragment barcoding.

Example 26. Enabling scATAC-Seq with CBP Nuclei Labeling

In situ ATAC-seq protocols are adapted to enable generation in situATAC-Seq protocols compatible with cellular barcode (CBP) and Spatialbarcode labeling. Namely, using methods described in US 2019/0032128A1and by Mimitou et al, scATAC-Seq incorporating CBP labels can beperformed concomitantly with scRNA-Seq and scProt-Seq.

Example 27. Sample Pre-Indexing Allows More than One Cell to Load in OneDroplet During Compartmentalization Step

The typical single-cell platforms require no more than one cellencapsulated in one droplet. Data from droplets containing two or morecells are discarded. However, multiple cells can be loaded in onedroplet if they are pre-indexed before droplet encapsulation and can bedemultiplexed after sequencing. One strategy is to split the cell sampleinto multiple pools and label cell transcriptomes in each pool withprimers containing sample barcodes during reverse transcription(Datlinger, P., et al. (2021) Ultra-high-throughput single-cell RNAsequencing and perturbation screening with combinatorial fluidicindexing. Nat Methods, 18, 635-642). Alternatively, cell hashing, asdescribed by Stokeus et al., can be employed to add sample “hashing”barcodes to the cell via barcoded antibodies that bind cell surfacemarkers such as CD45, CD98, CD44, and CD11a (Stoeckius, et al., 2018.“Cell Hashing with Barcoded Antibodies Enables Multiplexing and DoubletDetection for Single Cell Genomics.” Genome Biology 19 (1): 224). Duringlater stage emulsion PCR, these sample “hash” barcodes can be fused tothe CBP sequences to enable identification of the single cell and itsample of origin. Next, cells containing sample indexed macromoleculesor cells with sample hash barcoded antibodies bound to surface markersare pooled, randomly mixed, and encapsulated using a standardmicrofluidic droplet generator, such that most droplets are filled, andmultiple cells could occupy the same droplet. The numbers of cellsencapsulated in individual droplets are controlled so that chances oftwo cells carrying the same sample barcode are small. Inside thedroplets, macromolecules (such as RNA transcripts) are labeled with theamplified cell barcodes. Although cells in the same droplet share thesame cell barcode, the sample barcodes incorporated during the reversetranscription are distinct. As a result, the combination of the cellbarcode and sample barcode uniquely identifies single cells.

During the NGPA workflow for analysis of polypeptide macromolecules, therecording tag (R-tag) containing sample barcode is employed to labeldifferent sample pools. The barcoded samples are then pooled andprocessed as a single sample. After antibody binding and coding tag(C-Tag) information transfer (see Example 24), the cells carryingprotein identity and quantitation information are encapsulated andlabeled with cell barcodes in droplets as described above. In thissituation the sample barcode introduced in the R-tag is used todistinguish cells in the same droplets.

Example 28. DNA-Binding Protein Design and Use for CBP Labeling in Fixedand Permeabilized Cells

A designed TALE protein (dTALE) is designed to bind to the human genomictarget region from chr7 at chromosomal location: 63367837 to 63/367,857(AT-GAGTTTCTGGGACTGACGGT, SEQ ID NO: 3). The AT sequence lies outsidebinding region but serves as an AT dinucleotide region for downstreampsoralen crosslinking. The sequence of the dTALE protein is based onAvrXa10 (Cuculis, et al., 2020. “Divalent Cations Promote TALEDNA-Binding Specificity.” Nucleic Acids Research 48 (3): 1406-22). TheCBS sequence is attached to dTALE via a SpyCatcher Fusion which links toa SpyTag-CBP sequence (see FIG. 8C, where dCas9 is replaced with dTALE).The psoralen moiety is comprised of psoralen-TEG-azide (BiosearchTechnologies), and attached to synthetic alkyne lysine amino acid (zN6-((Prop-2-yn-1-yloxy)carbonyl)-L-lysine hydrochloride) on the SpyTagpeptide using standard click chemistry bioconjugation techniques.

The dTALE is designed to target 20-mer sequence from human chr7 using atandem series of 19.5 RVD repeats. SpyCatcher can be appended to the Nor C terminus of the dTALE. The core sequence of the dTALE is (RVDdipeptides shown in bold code for binding to the DNA sequenceGAGTTTCTGGGACTGACGGT, SEQ ID NO: 3):

SEQ ID NO: 4 MGPLCTPSRSSHHHHHHSSGLVPRGSHMLDTSLLDSMPAVGTPHTAAAPAECDEVQS GLRAA DDPPPTVRVAVTAARPPRAKPAPRRRAAQPSDASPAAQVDLRTLGYSQQQQEKIKPKVRSTVAQ TYQDIIRALPEATHEDIVGVGKQWSGARALEALLTEAGELRGPPLQLDTGQLLKIAKRGGVTAV EAVHAWRNALTGAPLNLTPDQVVAIASNIGGKQALETVQRLLPVLCQDHG LTPDQVVAIASNNGGKQALETVQRLLPVLCQDHGLTPDQVVAIASNIGGKQALETVQRLLPVLCQDHG LTPDQVVAIASNNGGKQALETVQRLLPVLCQDHGLTPDQVVAIASNGGGKQALETVQRLLPVLCQDHG LTPDQVVAIASNGGGKQALETVQRLLPVLCQDHGLTPDQVVAIASNGGGKQALETVQRLLPVLCQDHG LTPDQVVAIASHDGGKQALETVQRLLPVLCQDHGLTPDQVVAIASNGGGKQALETVQRLLPVLCQDHG LTPDQVVAIASNNGGKQALETVQRLLPVLCQDHGLTPDQVVAIASNNGGKQALETVQRLLPVLCQDHG LTPDQVVAIASNNGGKQALETVQRLLPVLCQDHGLTPDQVVAIASNIGGKQALETVQRLLPVLCQDHG LTPDQVVAIASHDGGKQALETVQRLLPVLCQDHGLTPDQVVAIASNGGGKQALETVQRLLPVLCQDHG LTPDQVVAIASNNGGKQALETVQRLLPVLCQDHGLTPDQVVAIASNIGGKQALETVQRLLPVLCQDHG LTPDQVVAIASHDGGKQALETVQRLLPVLCQDHGLTPDQVVAIASNNGGKQALETVQRLLPVLCQDHG LTPDQVVAIASNNGGKQALETVQRLLPVLCQDHGLTPDQVVAIASNG GGKQALESIVAQLSRPDPALA ALTNDHLVALACLGGRPALDAVKKGLPHAPELIRRINRRIPERTSHRVA,

The dTALE protein is expressed an purified as described in Cuculus etal., 2020, “Divalent Cations Promote TALE DNA-Binding Specificity.”Nucleic Acids Research 48 (3): 1406-22. The binding of the dTALE proteinis accomplished as follows: fixed and permeabilized cells are incubatedin 20 mM Tris-Cl buffer, pH 7.5, supplemented with 50 mM KCl, 10 mMMgCl2, 0.1% Tween-20, and 100 nM CBP-labeled dTALE protein at 30° C. for30 min. After binding and washing, psoralen crosslinking is achieved byexposing the cells to long wavelength UV light, wherein the intercalatedpsoralen moiety cross-links the two thymidine bases located on opposingDNA strands (Bornet et al. 1995). The optimal UV exposure is 6 J/cm2 of365 nm (long UV) applied directly to the cells placed in shallow wellson ice.

Example 29. Isolation of Nuclei from Cells Suspensions

As described by Massoni-Badosa et al. (Massoni-Badosa, et al., 2020.“Sampling Time-Dependent Artifacts in Single-Cell Genomics Studies.”Genome Biology 21 (1): 112), nuclei are isolated starting with an inputof ˜0.3-1.0×10{circumflex over ( )}6 cells in a 1.5 ml microcentrifugetube and centrifuged at 500×g for 5 min at 4° C. The supernatant isremoved, and 100 μl of chilled Lysis Buffer (10 mM Tris-HCl (pH 7.4); 10mM NaCl; 3 MgCl2; 0.1% Tween-20; 0.1% Nonidet P40 Substitute; 0.01%Digitonin and 1% BSA) is added and pipette-mixed about 10 times. Samplesare then incubated on ice during 3 min. Following lysis, 1 mL of chilledWash Buffer (10 mM Tris-HCl (pH 7.4); 10 mM NaCl; 3 MgCl2; 0.1% Tween-20and 1% BSA) is added and pipette mixed. Nuclei are centrifuged at 500×gfor 5 min at 4° C. to create a nuclear pellet. After removal of thesupernatant, nuclei are resuspended in 1×PBS buffer for furtherprocessing. Isolated nuclei can be used instead of cells in the examplesand methods disclosed above.

Example 30. Improving Specificity of CBP Probes to Target gDNA Loci byEmploying in Situ Hybridization and Ligation of Proximity Probes

The use of two or more proximity probes which anneal adjacent or nearbyto each other (gapped probes) on the target gDNA locus can generate aligated CBP probe product with improved specificity relative to the useof a single probe. The ligation product from the proximity probes can beformed directly by ligation of adjacent probes, or by a gap-fillligation step for gapped probes. In addition, one can employ more thantwo probes in a proximity-ligation approach as well to enhancespecificity. Ligation of adjacent or gap-extended probes requires aphosphate moiety on one terminus (typically 5′) and a hydroxyl moiety onthe other terminus (typically 3′) at the ligation junction. In somecases, the terminus phosphorylation requirement is to be reversed usingRtcB ligases (Das, et al., 2013. “Rewriting the Rules for End Joiningvia Enzymatic Splicing of DNA 3′-PO4 and 5′-OH Ends.” Proceedings of theNational Academy of Sciences of the United States of America 110 (51):20437-42) or via phosphoramidite chemical ligation (3′ phosphate; 5′amine). Additionally, a chemical ligation reaction between proximityprobes comprised of 3′-propargyl and 5′ amine termini at the ligationjunction can be joined using CuAAC reaction to ligate the two proximityprobes (El-Sagheer et al., 2017. “Single Tube Gene Synthesis byPhosphoramidate Chemical Ligation.” Chemical Communications 53 (77):10700-702).

In some embodiments of proximity probe ligation, two nucleic acid probesare designed to anneal adjacent to each other on a target gDNA locus. Ina preferred embodiment, the two probes are designed to a non-transcribedregion of a single copy locus to prevent interfering signal fromtranscribed RNA. In brief, cells or tissue sections are fixed andpermeabilized as described in Examples 2-4. A pair of CBP proximityprobes are annealed to the fixed and permeabilized cells/tissue. Namely,the CBP iFISH probe sequences described in Example 5 are modified to actas sequences for proximity ligation probes. In some preferredembodiments, the upstream and downstream GBS sequence arms of the CBPprobe have 17-30 bases of homology with single copy genomic loci,preferably a non-transcribed and non-repetitive region. Namely the iFISHprobe: CBP_Ch11-344380; TGGCCAGGAGGAGACTCTTCCAGGTCTCCCTTCTGACACC (SEQ IDNO: 5) can be used to generate a pair of proximity-ligation probes bysplitting the GBS region into an upstream assay arm (underlined 20bases) and downstream assay arm (bolded 20 bases)

(SEQ ID NO: 5) (5′-TGGCCAGGAGGAGACTCTTC CAGGTCTCCCTTCTGACACC-3′to create the following pair of GBS proximity probes: CBP_Ch11-344380-Up(5′-X . . . X-TGGCCAGGAGGAGACTCTTC-3′OH; SEQ ID NO: 6) andCBP_Ch11-344380-Down (5′-Phos-CAGGTCTCCCTTCTGACACC-X . . . X-3′OH; SEQID NO: 7). The X . . . X represents additional functional sequenceelements (e.g., PCR priming sites, UMIs, cellular barcodes, spatialbarcodes, and other barcodes) added to either or both the Upstreamand/or Downstream GBS sequences to constitute the pair of proximity CBPprobes. A similar pair of proximity CBP probes can be generated from theExample 5 iFISH probe sequence containing a PmeI site: Chr7 CBP:AAACCTTGCCAACCATGAGTTTCTGGGACTGACGGTGATG (SEQ ID NO: 2). Target gDNAsequence: chr7, from 63/367,821 to 63/367,861. Namely, the two CBPproximity probes derived from the iFISH probe are: 5′-X . . .X-AAACCTTGCCAACCATGAGT (SEQ ID NO: 8) and 5′-Phos-TTCTGGGACTGACGGTGATG-X. . . X (SEQ ID NO: 9). Again, X . . . X represents additionalfunctional sequence elements as described above.

In situ hybridization of the paired CBP proximity probes to gDNA isfacilitated by generation of single stranded DNA in the gDNA targetregion. This can be accomplished by methods as described in Example 8using denaturation, strand invasion, and/or linearization approaches.Ligation and gap-fill ligation conditions similar to what is describedin Example 9 are used to ligate the upstream and downstream CBP probesto form a complete CBP sequence for subsequent amplification and CBPlabeling of cellular analytes.

Example 31. Labeling of Cellular Protein Analytes with AmplifiedgDNA-Associated CBP Probes

Cellular protein molecules are denatured, and the F-amine group oflysine residues (K) is chemically conjugated to an activated universalDNA tag molecule that serves as a primer or ligation acceptor site froman amplified CBP probe. A two-step bioconjugation process is used tofirst attach a heterobifunctional linker comprised of an amine-reactiveNHS moiety, a PEG or alkane linker, and an orthogonal reactive couplinghandle. After coupling the heterobifunctional linker, an activated DNAtag stub is conjugated to the reactive handle. In this particularinstance, NHS-PEG12-mTet, is used to activate the lysine F-amine groupwith an orthogonal reactive coupling handle, methyl tetrazine (mTet).The DNA tag is comprised of a 5′ TCO moiety which readily couples tomTet via an iEDDA reaction. Excess DNA tag is washed away aftercoupling.

Sequence information from the amplified CBP probe is transferred to theDNA stub during a PCR amplification step. The DNA stub attached to theproteins acts as one primer (a small amount of free primer can also beused to enhance the amplification reaction) and an exogenously addedprimer is used as the second primer in the PCR reaction.

Exemplary workflow is shown in FIG. 15 . After barcoding, individualcells are compartmentalized in droplets, followed by cell barcodeamplification, transfer barcode information to rTags of proteinanalytes, and exemplary NGPA assay for the tagged protein analytes. Thefollowing steps can be performed using standard methods known in the artor disclosed above. (A) Single cells are fixed, permeabilized, and havetheir nuclei labeled with CBPs. (B) Single cells are encapsulated indroplets along with a polymerizable matrix and lysis buffer (forspecific method conditions, see US 20190145982 A1; Tamminen and Virta2015; Spencer, Tamminen et al. 2016). (C) Polymer matrix polymerizes andimmobilizes DNA rTags within matrix. (D) Proteins released from the cellare conjugated to activated DNA rTags within polymer matrix. (E) Singlecell polymer beads (SCPB) are extracted into aqueous phase andcombinatorial barcodes can be added to SCPBs via a SCI-Seq split-poolprocess, as described in U.S. Ser. No. 10/144,950 B2; US20180273933 A1;O'Huallachain, et al., 2020, “Ultra-High Throughput Single-Cell Analysisof Proteins and RNAs by Split-Pool Synthesis.” Communications Biology 3(1): 1-19. (F) The resultant SCPBs can be used directly in a ProteoCodeNGPA immunoassay (exemplary antibody readout shown) or processed for anNGPS assay for quantitative assessment of proteins from single cell.

Example 32. Amplification of Exemplary Polynucleotide Cell BarcodeProbes by “Bridge” Amplification Using a Pair of Primers Attached toPorous Sepharose Beads

To demonstrate amplification of polynucleotide barcode probes withinpermeabilized cells and/or nuclei by primers covalently attached tocomponents of the permeabilized cells and/or nuclei, the following modelexperiment was performed (see FIG. 16A-B). An on-bead “bridge”amplification system was used comprising porous sepharose beadscomprising two primers attached to their surfaces, namely P5 primer(5′-AATGATACGGCGACCACCGA-3′-SEQ ID NO: 10) and P7 primer(5′-CAAGCAGAAGACGGCATACGAGAT-3′-SEQ ID NO: 11). Probe amplification onthese beads using attached primers models amplification in permeabilizedcells and/or nuclei.

P5 and P7 oligonucleotides (primers) were derivatized withtrans-cyclooctene (TCO) and chemically immobilized on beads(NHS-Activated Sepharose High Performance, Cytiva, USA) modified withmethyltetrazine (mTet) using TCO-mTet click chemistry. The densities ofthe P5 and P7 primers on beads were controlled by passivation asfollows. A mixture of mTet-PEG-NHS and methyl-PEG-NHS was resuspended at1 mM in DMSO and incubated with amine beads at room temperatureovernight. The ratio of the Methyl to mTet PEG was titrated to adjustthe final mTet surface density on the beads. Three different mTetdensities were employed: 100 mM, 10 mM and 1 mM. Unreacted amine groupswere capped with a mixture of 0.1M acetic anhydride and 0.1M DIEA in DMF(500 ul for 10 mg of beads) at room temperature for 2 hrs. After cappingand washing 3 times in DMF, the beads were resuspended in phosphatecoupling buffer at 10 mg/ml. TCO-P5 and TCO-P7 oligonucleotides werereacted with bead-immobilized mTet by the click chemistry reaction.

The beads with immobilized P5 and P7 primers were contacted with ˜300 bppolynucleotide barcode probes each comprising one terminaloligonucleotide region complementary to P5 primer and another terminaloligonucleotide region complementary to P7 primer. The beads weresubjected to PCR (conditions: 94° C. for 2 min, then [98° C. 20 s, 67°C. 30 s, 72° C. 1 min]×25 cycles) using 10,000 beads (having 100 mMmTet, 10 mM mTet, 1 mM mTet, or Negative Control (no mTet)) per reactionwith a titration of the supplied polynucleotide barcode probes (500 μM-1fM). Following PCR, bridge amplification effectiveness was measured byqPCR (KAPA Library Quantification Complete Universal Kit, Roche) todetect the amount of product formation on bead-bound tags. ResultingqPCR data was used for amplified probe quantification. The data areshown in Table 1 and in FIG. 16A-B.

TABLE 1 qPCR quantification of the amplified probes. qPCR quantification(nM) 100 mM 10 mM 1 mM Neg Input DNA mTet mTet mTet Ctrl 500 pM38,070.710 9,859.871 1,443.692 45.936 100 pM 56,317.880 6,896.521513.707 4.656  20 pM 19,999.697 4,893.717 53.631 0.527  4 pM 32,612.860918.246 15.969 0.108 Negative-1 0.044 0.001 0.002 0.012  1 pM 298.41419.419 2.960 0.368 100 pM 99.644 1.367 0.260 0.043  10 pM 3.503 0.1490.029 0.007   1 pM 1.605 0.085 0.012 0.002 Negative-2 0.001 0.000 0.0010.001

The present disclosure is not intended to be limited in scope to theparticular disclosed embodiments, which are provided, for example, toillustrate various aspects of the invention. Various modifications tothe compositions and methods described will become apparent from thedescription and teachings herein. Such variations may be practicedwithout departing from the true scope and spirit of the disclosure andare intended to fall within the scope of the present disclosure. Theseand other changes can be made to the embodiments in light of theabove-detailed description. In general, in the following claims, theterms used should not be construed to limit the claims to the specificembodiments disclosed in the specification and the claims, but should beconstrued to include all possible embodiments along with the full scopeof equivalents to which such claims are entitled. Accordingly, theclaims are not limited by the disclosure.

1-41. (canceled)
 42. A method for barcoding macromolecules from a samplecomprising a population of cells, the method comprising the followingsteps: a) permeabilizing cells, and/or nuclei of the cells, from thepopulation of cells of the sample; b) optionally making genomic DNA ofthe permeabilized cells and/or nuclei at least partially accessible tonucleic acid hybridization; c) delivering cell barcode probes to thepermeabilized cells and/or nuclei of the permeabilized cells, wherein agiven cell barcode probe comprises a genome binding element shared amongthe cell barcode probes, and a cell barcode unique for the given cellbarcode probe, and wherein the genome binding element hybridizes to aregion in the genomic DNA, thereby forming a nucleic acid duplex betweenthe genome binding element and the region of the genomic DNA in thecells and/or nuclei; d) removing cell barcode probes that are not boundto the genomic DNA from the cells and/or nuclei, whereby no more than adefined number of copies of the cell barcode probe remain in each cellor nucleus; e) partitioning the cells and/or nuclei into a plurality ofcompartments; f) amplifying the cell barcodes within compartments of theplurality of compartments, thereby forming amplified cell barcodeswithin the compartments; and g) attaching the amplified cell barcodes tothe macromolecules within the compartments, thereby forming barcodedmacromolecules.
 43. The method of claim 42, further comprising releasingthe barcoded macromolecules from the compartments.
 44. The method ofclaim 42, wherein the macromolecules being barcoded are polypeptides,mRNA molecules or cDNA molecules.
 45. The method of claim 42, whereinthe region in the genomic DNA is a non-repetitive region.
 46. The methodof claim 42, wherein the non-repetitive region in the genomic DNA is anon-coding region or a differentially methylated region.
 47. The methodof claim 42, wherein the defined number of copies is one copy.
 48. Themethod of claim 42, wherein the defined number of copies is two copies.49. The method of claim 42, wherein the sample is a spatial sample, andwherein the sample is dissociated into a plurality of cells at step (e).50. The method of claim 49, wherein each of the cell barcode probesfurther comprise a positional barcode different for at least some of thecell barcode probes.
 51. The method of claim 49, wherein the cellbarcode probes are delivered at step (c) from a spatially ordered array.52. The method of claim 49, further comprising, after step (b), (i)delivering a plurality of positional probes to the permeabilized cellsand/or nuclei, wherein a given positional probe comprises a commontargeting element configured to be attached to the macromolecules and apositional barcode different for each positional probes; and (ii)attaching positional probes from the plurality of positional probes tothe macromolecules.
 53. The method of claim 52, wherein each of theamplified cell barcodes comprises a common region that is configured tohybridize to a region in the positional probes; and the method furthercomprises a step of performing a primer extension reaction to transferthe amplified cell barcodes to the positional probes attached to themacromolecules.
 54. The method of claim 52, wherein the plurality ofpositional probes is delivered from a spatially ordered array.
 55. Themethod of claim 42, wherein each compartment of the plurality ofcompartments comprises a compartment barcode configured to be attachedto the macromolecules.
 56. The method of claim 42, wherein duringpartitioning the cells and/or nuclei into the plurality of compartmentsat step (e), on average no more than one cell or nucleus comprising acell barcode probe is comprised within a single compartment.
 57. Themethod of claim 42, wherein attaching the amplified cell barcodes to themacromolecules within the compartments comprises: i) covalentlyattaching nucleic acid recording tags to the macromolecules ormacromolecule derivatives of the cell; and (ii) attaching the amplifiedcell barcodes to the nucleic acid recording tags.
 58. A method forbarcoding macromolecules from a sample comprising a population of cells,the method comprising the following steps: a) permeabilizing cells,and/or nuclei of the cells, from the population of cells of the sample;b) delivering reactive primers that are configured to be covalentlyattached to components of the permeabilized cells and/or nuclei, therebycreating a plurality of attached primers; c) optionally making genomicDNA of the permeabilized cells and/or nuclei at least partiallyaccessible to nucleic acid hybridization; d) delivering cell barcodeprobes to the permeabilized cells and/or nuclei of the permeabilizedcells, wherein a given cell barcode probe comprises a genome bindingelement shared among the cell barcode probes, and a cell barcode uniquefor the given cell barcode probe, and wherein the genome binding elementhybridizes to a region in the genomic DNA, thereby forming a nucleicacid duplex between the genome binding element and the region of thegenomic DNA in the cells and/or nuclei; e) removing cell barcode probesthat are not bound to the genomic DNA from the cells and/or nuclei,whereby no more than a defined number of copies of the cell barcodeprobe remain in each cell or nucleus; amplifying the cell barcodes usingthe plurality of attached primers, thereby forming amplified cellbarcodes within the compartments; and attaching the amplified cellbarcodes to the macromolecules within cells, thereby forming barcodedmacromolecules.
 59. The method of claim 58, wherein amplifying the cellbarcodes at step (f) comprises providing conditions for hybridizationbetween the cell barcode probes and the plurality of attached primers.60. The method of claim 58, wherein the defined number of copies is onecopy.
 61. The method of claim 58, wherein the region in the genomic DNAis a non-repetitive region.
 62. A method for barcoding macromoleculesfrom a sample comprising a population of cells, the method comprisingthe following steps: a) permeabilizing cells, and/or nuclei of thecells, from the population of cells of the sample; b) delivering aspecific genomic DNA-binding carrier comprising a cell barcode probe tothe permeabilized cells and/or nuclei, wherein a given cell barcodeprobe comprises a cell barcode unique for each cell or nucleus, and apriming site, and wherein the specific genomic DNA-binding carrierspecifically binds to a region in the genomic DNA of the cells and/ornuclei; c) removing specific genomic DNA-binding carriers that are notbound to the genomic DNA from the cells and/or nuclei, whereby no morethan a defined number of copies of the cell barcode probe remain in eachcell or nucleus; d) amplifying the cell barcodes that were not removedfrom the cells and/or nuclei at step (c), thereby forming amplified cellbarcodes; and e) attaching the amplified cell barcodes to themacromolecules, thereby forming barcoded macromolecules.
 63. The methodof claim 62, wherein step (d) comprises the following steps: (i)partitioning the cells and/or nuclei into a plurality of compartments;(ii) amplifying the cell barcodes within compartments of the pluralityof compartments, thereby forming amplified cell barcodes within thecompartments.
 64. The method of claim 62, wherein the defined number ofcopies is one copy.